Prosecution Insights
Last updated: July 17, 2026
Application No. 18/413,922

SYSTEMS AND METHODS FOR TISSUE REMOVAL

Final Rejection §102§103§112
Filed
Jan 16, 2024
Priority
Jan 22, 2016 — provisional 62/281,820 +2 more
Examiner
FISHER, VICTORIA HICKS
Art Unit
3786
Tech Center
3700 — Mechanical Engineering & Manufacturing
Assignee
Applied Medical Resources Corporation
OA Round
2 (Final)
41%
Grant Probability
Moderate
3-4
OA Rounds
1y 8m
Est. Remaining
79%
With Interview

Examiner Intelligence

Grants 41% of resolved cases
41%
Career Allowance Rate
279 granted / 686 resolved
-29.3% vs TC avg
Strong +38% interview lift
Without
With
+38.1%
Interview Lift
resolved cases with interview
Typical timeline
4y 2m
Avg Prosecution
45 currently pending
Career history
747
Total Applications
across all art units

Statute-Specific Performance

§101
3.5%
-36.5% vs TC avg
§103
65.1%
+25.1% vs TC avg
§102
6.2%
-33.8% vs TC avg
§112
24.3%
-15.7% vs TC avg
Black line = Tech Center average estimate • Based on career data from 686 resolved cases

Office Action

§102 §103 §112
DETAILED ACTION This action is in response to the amendment filed 1/27/2026. Currently, claims 1-3, 6, 7 and 9-23 are pending in the application. Claims 4, 5 and 8 are cancelled by Applicant. New claims 21-23 are added by applicant. Notice of Pre-AIA or AIA Status The present application, filed on or after March 16, 2013, is being examined under the first inventor to file provisions of the AIA . Response to Arguments Applicant’s amendment to claim 6 is sufficient to overcome the previous objection to claim 6. Applicant’s amendment to claim 9 is sufficient to overcome the previous objection to claim 9. Applicant’s amendment to the specification is sufficient to overcome the previous objection to claim 19. Applicant’s amendment to claim 3 is sufficient to overcome the previous rejection of claim 3 under 35 U.S.C. 112(b) or 35 U.S.C. 112 (pre-AIA ), second paragraph. Applicant’s amendment to claim 9 is sufficient to overcome the previous rejection of claim 9 under 35 U.S.C. 112(b) or 35 U.S.C. 112 (pre-AIA ), second paragraph. Applicant’s amendment to claim 17 is sufficient to overcome the previous rejection of claim 17 under 35 U.S.C. 112(b) or 35 U.S.C. 112 (pre-AIA ), second paragraph. Applicant's arguments filed 1/27/2026 have been fully considered but they are not persuasive. In response to Applicant’s argument that Smith does not teach a batten configured to stiffen and reinforce a side section of the guard portion to facilitate insertion of the surgical shield into the orifice, the examiner respectfully disagrees. As detailed below, Smith teaches a batten (elongate member 140) configured to stiffen and reinforce ([0025] teaches “an elongate member 140 insertable into tube 130;” [0027] teaches “elongate member 140 is made of a semi-rigid material” and “when inserted, elongate member 140 provides additional rigidity to tube 130;” when inserted into tube 130, the semi-rigid elongate member 140 provides structural support to increase the rigidity of the tube 130 and stiffen and reinforce the structure thereof) a side section (tube 130; Figure 1 teaches the tube 130 being positioned on the lateral outer surface 118 of housing 110) of the guard portion (housing 110, tube 130) to facilitate insertion of the surgical shield (surgical device 100) into ([0025] teaches “an elongate member 140 insertable into tube 130;” the elongate member 140 is capable of being inserted into tube 130 before insertion of the surgical device 100 into tissue T such that the elongate member 140 provides a semi-rigid handle to stabilize movement of the surgical device during insertion) the orifice ([0027] teaches “distal end 114 of housing 110 to be secured against an inner surface of tissue ‘T’”). In response to applicant's argument that Smith teaches the elongate member 140 being positioned within tube 130 after insertion of the device within the tissue and not before/during insertion as claimed, the examiner notes that a recitation of the intended use of the claimed invention must result in a structural difference between the claimed invention and the prior art in order to patentably distinguish the claimed invention from the prior art. If the prior art structure is capable of performing the intended use, then it meets the claim. In the present case, the elongate member 140 is capable of being inserted into tube 130 before insertion of the surgical device 100 into tissue T such that the elongate member 140 provides a semi-rigid handle to stabilize movement of the surgical device during insertion. Claim Rejections - 35 USC § 112 The following is a quotation of the first paragraph of 35 U.S.C. 112(a): (a) IN GENERAL.—The specification shall contain a written description of the invention, and of the manner and process of making and using it, in such full, clear, concise, and exact terms as to enable any person skilled in the art to which it pertains, or with which it is most nearly connected, to make and use the same, and shall set forth the best mode contemplated by the inventor or joint inventor of carrying out the invention. The following is a quotation of the first paragraph of pre-AIA 35 U.S.C. 112: The specification shall contain a written description of the invention, and of the manner and process of making and using it, in such full, clear, concise, and exact terms as to enable any person skilled in the art to which it pertains, or with which it is most nearly connected, to make and use the same, and shall set forth the best mode contemplated by the inventor of carrying out his invention. Claims 1-3, 6, 7 and 9-23 are rejected under 35 U.S.C. 112(a) or 35 U.S.C. 112 (pre-AIA ), first paragraph, as failing to comply with the written description requirement. The claim(s) contains subject matter which was not described in the specification in such a way as to reasonably convey to one skilled in the relevant art that the inventor or a joint inventor, or for applications subject to pre-AIA 35 U.S.C. 112, the inventor(s), at the time the application was filed, had possession of the claimed invention. Claims 1 recites “distal end of the reinforcing portion is positioned forward of the guard portion in an insertion direction.” No support is provided for this claim limitation in Applicant’s specification as originally filed. Applicant’s original disclosure explicitly teaches the distal end of the reinforcing portion being positioned within the guard portion, and not forward of the guard portion as claimed. This is clearly shown in Figure 189A of Applicant’s disclosure. Additionally, see at least [0446] of the publication of the present application, which teaches “the top of the guard portion 7002 includes a channel 7024 that is sized and configured to receive the batten 7004” and “the batten 7004 may be inserted into the channel 7024 for the insertion of the shield 7000.” Thus, it is clear that the reinforcing portion 7026 of the batten 7004 is positioned within the guard portion 7002, and not forward of the guard portion 7002 as claimed. Claims 2, 3, 6, 7 and 9-23 depend on claim 1 and therefore, include the same error. Claim 9 is rejected under 35 U.S.C. 112(a) or 35 U.S.C. 112 (pre-AIA ), first paragraph, as failing to comply with the written description requirement. The claim(s) contains subject matter which was not described in the specification in such a way as to reasonably convey to one skilled in the relevant art that the inventor or a joint inventor, or for applications subject to pre-AIA 35 U.S.C. 112, the inventor(s), at the time the application was filed, had possession of the claimed invention. Claim 9 recites “the batten is L-shaped such that the handle portion is perpendicular to the reinforcing portion.” No support is provided for this claim limitation in Applicant’s specification as originally filed. While Applicant’s disclosure teaches the handle portion 7028 of the batten 7004 being angles relative to the reinforcing portion 7026 thereof (see Applicant’s Figure 189A, for instance), this angle is not shown or taught to be a perpendicular (90 degree) angle as claimed. Figure 189A, for instance, teaches the reinforcing portion 7026 being bowed outward from the handle portion 7028 such that the angle between the reinforcing portion 7026 and the handle portion 7028 is greater than 90 degrees. Claim 23 is rejected under 35 U.S.C. 112(a) or 35 U.S.C. 112 (pre-AIA ), first paragraph, as failing to comply with the written description requirement. The claim(s) contains subject matter which was not described in the specification in such a way as to reasonably convey to one skilled in the relevant art that the inventor or a joint inventor, or for applications subject to pre-AIA 35 U.S.C. 112, the inventor(s), at the time the application was filed, had possession of the claimed invention. Claim 23 recites “a leading distal insertion angle is defined by a projection of a distal plane containing the distal opening and a plane perpendicular to a lateral axis of the guard portion.” No support is provided for this claim limitation in Applicant’s specification as originally filed. As shown in at least Applicant’s Figure 188, the leading distal insertion angle is defined by a projection of a distal plane containing the distal opening and the lateral axis of the guard portion. The following is a quotation of 35 U.S.C. 112(b): (b) CONCLUSION.—The specification shall conclude with one or more claims particularly pointing out and distinctly claiming the subject matter which the inventor or a joint inventor regards as the invention. The following is a quotation of 35 U.S.C. 112 (pre-AIA ), second paragraph: The specification shall conclude with one or more claims particularly pointing out and distinctly claiming the subject matter which the applicant regards as his invention. Claim 21 is rejected under 35 U.S.C. 112(b) or 35 U.S.C. 112 (pre-AIA ), second paragraph, as being indefinite for failing to particularly point out and distinctly claim the subject matter which the inventor or a joint inventor (or for applications subject to pre-AIA 35 U.S.C. 112, the applicant), regards as the invention. Regarding claim 21, the term "pendulum-like" renders the claim(s) indefinite because the claim(s) include(s) elements not actually disclosed (those encompassed by "-like"), thereby rendering the scope of the claim(s) unascertainable. See MPEP § 2173.05(d). Claim 22 is rejected under 35 U.S.C. 112(b) or 35 U.S.C. 112 (pre-AIA ), second paragraph, as being indefinite for failing to particularly point out and distinctly claim the subject matter which the inventor or a joint inventor (or for applications subject to pre-AIA 35 U.S.C. 112, the applicant), regards as the invention. Regarding claim 22, the term "wedge-like" renders the claim(s) indefinite because the claim(s) include(s) elements not actually disclosed (those encompassed by "-like"), thereby rendering the scope of the claim(s) unascertainable. See MPEP § 2173.05(d). Claim Rejections - 35 USC § 102 The following is a quotation of the appropriate paragraphs of 35 U.S.C. 102 that form the basis for the rejections under this section made in this Office action: A person shall be entitled to a patent unless – (a)(1) the claimed invention was patented, described in a printed publication, or in public use, on sale, or otherwise available to the public before the effective filing date of the claimed invention. Claim(s) 1-3, 6, 7, 10-16 and 18-23 is/are rejected under 35 U.S.C. 102(a)(1) as being anticipated by Smith (US 2012/0245429 A1). In regards to claim 1, Smith teaches in Figures 1-7, [0025] and [0027] a guard portion (housing 110, tube 130) formed of cut-resistant material (the housing 110 and tube 130 are taught in Figures 1-7 to be made of physical material(a) having a thickness, thus having a degree of resistance to cutting) and having a generally tubular shape (as shown in Figures 1-7, housing 110 has a tubular structure with lumen 116 extending therethrough; [0025] teaches “housing 110 may also define a lumen 116 extending longitudinally therethrough”) having an inner surface (interior surface of housing 110) and an outer surface (exterior surface of housing 110) defining a thickness therebetween (as shown in Figure 1); the guard portion (housing 110, tube 130) defining a lumen (lumen 116) extending along a longitudinal axis ([0025] teaches “housing 110 may also define a lumen 116 extending longitudinally therethrough”) between (extending between, as shown in Figure 1) a proximal opening (opening of lumen 116 positioned in proximal end 112; see Figure 1) at a proximal end (proximal end 112) and a distal opening (opening of lumen 116 positioned in distal end 114; see Figure 1) at a distal end (distal end 114); and a batten (elongate member 140) configured to stiffen and reinforce ([0025] teaches “an elongate member 140 insertable into tube 130;” [0027] teaches “elongate member 140 is made of a semi-rigid material” and “when inserted, elongate member 140 provides additional rigidity to tube 130;” when inserted into tube 130, the semi-rigid elongate member 140 provides structural support to increase the rigidity of the tube 130 and stiffen and reinforce the structure thereof) a side section (tube 130; Figure 1 teaches the tube 130 being positioned on the lateral outer surface 118 of housing 110) of the guard portion (housing 110, tube 130) to facilitate insertion of the surgical shield (surgical device 100) into ([0025] teaches “an elongate member 140 insertable into tube 130;” the elongate member 140 is capable of being inserted into tube 130 before insertion of the surgical device 100 into tissue T such that the elongate member 140 provides a semi-rigid handle to stabilize movement of the surgical device during insertion) the orifice ([0027] teaches “distal end 114 of housing 110 to be secured against an inner surface of tissue ‘T’”); the batten (elongate member 140) having a reinforcing portion (portion of elongate member 140 positioned within tube 130 in use; see Figure 5; [0025] teaches “an elongate member 140 insertable into tube 130”) connected to a handle portion (portion of elongate member 140 external to tube 130 in use; shown in Figure 5; can be considered a “handle” inasmuch as it is capable of being manually grasped); the reinforcing portion (portion of elongate member 140 positioned within tube 130 in use) being connected to (as shown in Figure 1; [0025] teaches “an elongate member 140 insertable into tube 130”) the side section (tube 130) of guard portion (housing 110, tube 130) and extending along (as shown in Figure 7) the longitudinal axis of ([0027] teaches “elongate member 140 is made of a semi-rigid material and may be inserted through longitudinal portion 132”) the guard portion (housing 110, tube 130) such that a distal end (distal tip 142) of the reinforcing portion (portion of elongate member 140 positioned within tube 130 in use) is positioned forward of the guard portion (housing 110, tube 130) in an insertion direction (Figure 1 teaches the distal tip 142 being positioned in front of housing 110 in a lateral direction that is capable of being positioned in the tissue T first during insertion); the handle portion (portion of elongate member 140 external to tube 130 in use) being located at (as shown in Figures 5 and 7) the proximal end (proximal end 112) of the guard portion (housing 110, tube 130) and extending away from (Figures 5 and 7 teach the portion of elongate member 140 external to tube 130 in use extending laterally away from the proximal end 112) the proximal end (proximal end 112) of the guard portion (housing 110, tube 130). In regards to claim 2, Smith teaches the apparatus of claim 1. Smith teaches in Figures 1 and 7, [0027] and [0029] that the guard portion (housing 110, tube 130) comprises a bead ([0029] teaches “elongate member 140 now circumnavigates distal end 114 of housing 110 thereby creating a ring similar to ring 122”) having an enlarged thickness (inasmuch as the distal ring 122 is shown in Figure 7 to flare outward and project laterally, increasing the width/thickness of surgical device 100) around (as shown in Figure 7) the distal opening (opening of lumen 116 positioned in distal end 114; see Figure 1). In regards to claim 3, Smith teaches the apparatus of claims 1 and 2. Smith teaches in Figures 1 and 7, [0027] and [0029] that the enlarged thickness (inasmuch as the distal ring 122 is shown in Figure 7 to flare outward and project laterally, increasing the width/thickness of surgical device 100) is non-uniform around (inasmuch as the distal ring 122 is shown in Figure 7 to flare outwardly and thus, forms a gradually increasing width/thickness of surgical device 100) the distal opening (opening of lumen 116 positioned in distal end 114; see Figure 1) such that, in a plane containing the distal opening (opening of lumen 116 positioned in distal end 114; see Figure 1), the thickness of the bead ([0029] teaches “elongate member 140 now circumnavigates distal end 114 of housing 110 thereby creating a ring similar to ring 122”) is more prominent (prominence of the thickness of the bead in a plane containing the opening of lumen 116 varies depending upon the point of view of the observer) along a top of the guard portion (housing 110, tube 130) relative to a bottom of the guard portion (housing 110, tube 130). In regards to claim 6, Smith teaches the apparatus of claim 1. Smith teaches in Figures 1-7 and [0027] that the distal opening (opening of lumen 116 positioned in distal end 114; see Figure 1) lies in a distal plane (the opening of lumen 116 positioned in distal end 114 lies in a substantially horizontal distal plane, as shown in Figure 1) that is angled (substantially perpendicularly) with respect to the longitudinal axis (vertical axis) to facilitate insertion of the distal end (distal end 114) of the surgical shield (surgical device 100) into the orifice of ([0027] teaches “distal end 114 of housing 110 to be secured against an inner surface of tissue ‘T’”) the patient (the angled corner ). In regards to claim 7, Smith teaches the apparatus of claim 1. Smith teaches in Figures 1-7 that the proximal opening (opening of lumen 116 positioned in proximal end 112; see Figure 1) lies in a proximal plane (the opening of lumen 116 positioned in distal end 114 lies in a substantially horizontal proximal plane, as shown in Figure 1) that is angled (substantially perpendicularly) with respect to the longitudinal axis (vertical axis) to create a flange (formed by the pointed corner where the housing 110 and proximal end 112 intersect) at the proximal end (proximal end 112). In regards to claim 10, Smith teaches the apparatus of claim 1. Smith teaches in Figures 1 and 7 that the lumen (lumen 116) has an elongate (inasmuch as it has a length) cross-section (shown in Figures 1 and 7) taken in a plane perpendicular to the longitudinal axis (vertical axis) at the proximal end (proximal end 112) and an elongate (inasmuch as it has a length) cross-section (shown in Figures 1 and 7) taken in a plane perpendicular to the longitudinal axis (vertical axis) at the distal end (distal end 114). In regards to claim 11, Smith teaches the apparatus of claims 1 and 10. Smith teaches in Figures 1 and 7 the lumen (lumen 116) has a circular cross-section between (as shown in Figures 1 and 7) the distal end (distal end 114) and proximal end (proximal end 112). In regards to claim 12, Smith teaches the apparatus of claim 1. Smith teaches in [0025] and Figures 1 and 7 a bead (ring 122; shown in Figure 7 to have a cross-section resembling the shape of a bead) around (as shown in Figure 7; [0027] teaches “a ring 122 circumnavigating proximal end 112”) the proximal opening (opening of lumen 116 positioned in proximal end 112; see Figure 1). In regards to claim 13, Smith teaches the apparatus of claim 1. Smith teaches in Figures 5 and 7 that the reinforcing portion (portion of elongate member 140 positioned within tube 130 in use) is curved so as to conform to (as shown in Figures 5 and 7, the portion of elongate member 140 positioned within tube 130 follows the curvature of the interior and exterior surfaces of housing 110) the shape of the inner (interior surface of housing 110) and outer (exterior surface of housing 110) surfaces of the guard portion (housing 110, tube 130). In regards to claim 14, Smith teaches the apparatus of claim 1. Smith teaches in Figure 5 that the outer surface (exterior surface of housing 110) of the guard portion (housing 110, tube 130) is curved concave along (as shown in Figure 5) the longitudinal axis (vertical axis) and the inner surface (interior surface of housing 110) of the guard portion (housing 110, tube 130) is conformingly curved convex (as shown in Figure 5). In regards to claim 15, Smith teaches the apparatus of claims 1 and 14. Smith teaches in Figure 5 that the reinforcing portion (portion of elongate member 140 positioned within tube 130 in use) is curved so as to have an outer surface (exterior, outward-facing surface) that is concave along a length (as shown in Figure 5) of the reinforcing portion (portion of elongate member 140 positioned within tube 130 in use) and is convex along a width (as shown in Figure 5) of the reinforcing portion (portion of elongate member 140 positioned within tube 130 in use). In regards to claim 16, Smith teaches the apparatus of claims 1 and 14. Smith teaches in Figure 5 that the reinforcing portion (portion of elongate member 140 positioned within tube 130 in use) is curved so as to have an inner surface (interior surface) that is convex along a length (as shown in Figure 5) of the reinforcing portion (portion of elongate member 140 positioned within tube 130 in use) and is concave along a width (as shown in Figure 5) of the reinforcing portion (portion of elongate member 140 positioned within tube 130 in use). In regards to claim 18, Smith teaches the apparatus of claim 1. Smith teaches in [0025] and [0027] that the guard portion (housing 110, tube 130) is made of flexible material ([0025] teaches “housing 110 may be made of a bio-compatible material which is flexible or collapsible and designed to allow for flexibility or collapsibility during insertion”) and the batten (elongate member 140) is more rigid relative to ([0027] teaches “elongate member 140 is made of a semi-rigid material”) the guard portion (housing 110, tube 130). In regards to claim 19, Smith teaches the apparatus of claim 1. Smith teaches in Figure 1 that the guard portion (housing 110, tube 130) includes a depending flange portion (free end of tube 130) at (Figure 1 teaches the free end of tube 130 being positioned on the proximal end 112) the proximal end (proximal end 112). In regards to claim 20, Smith teaches the apparatus of claim 1. Smith teaches in Figure 5 that the guard portion (housing 110, tube 130) is substantially hourglass shaped (Figure 5 teaches the housing 110 being shaped like an hourglass). In regards to claim 21, Smith teaches the apparatus of claim 1. Smith teaches in Figures 1 and 7 that the surgical shield (surgical device 100), when positioned in the insertion direction, is configured to move in a pendulum-like manner about a proximal end (free end) of the handle portion (portion of elongate member 140 external to tube 130 in use) so as to create an arc-shaped pathway of insertion (as shown in Figures 1 and 7, the surgical device 100 is structured such that a user is capable of manually grasping the free end of the portion of elongate member 140 external to tube 130 in use and moving the surgical device in a pendulum-like manner to create an arc-shaped pathway of insertion). In regards to claim 22, Smith teaches the apparatus of claim 1. Smith teaches in Figure 1 that the distal end (distal tip 142) of the reinforcing portion (portion of elongate member 140 positioned within tube 130 in use; see Figure 5; [0025] teaches “an elongate member 140 insertable into tube 130”) at the distal end (distal end 114) of the guard portion (housing 110, tube 130) leads the insertion and serves as a leading end ([0027] teaches “distal end 114 of housing 110 to be secured against an inner surface of tissue ‘T’”) (distal tip 142 is capable of being used as a leading end to provide the first point of insertion of the device into the tissue T); the leading end of the guard portion (housing 110, tube 130) increasing in size in a proximal direction to form a wedge-like configuration having an acute angle, thereby facilitating tissue retraction during insertion (see angle defined in the annotated copy of Figure 7 provided below). In regards to claim 23, Smith teaches the apparatus of claim 1. Smith teaches in Figure 7 that a leading distal insertion angle (as defined in the annotated copy of Figure 7 provided below) is defined by (defined between, as shown in Figure 7) a projection of a distal plane (horizonal plane at the opening of lumen 116 positioned in distal end 114) containing the distal opening (opening of lumen 116 positioned in distal end 114; see Figure 1) and a plane (vertical plane, as defined in the annotated copy of Figure 7 provided below) perpendicular to a lateral axis (horizontal axis) of the guard portion (housing 110, tube 130). PNG media_image1.png 438 775 media_image1.png Greyscale Claim Rejections - 35 USC § 103 The following is a quotation of 35 U.S.C. 103 which forms the basis for all obviousness rejections set forth in this Office action: A patent for a claimed invention may not be obtained, notwithstanding that the claimed invention is not identically disclosed as set forth in section 102, if the differences between the claimed invention and the prior art are such that the claimed invention as a whole would have been obvious before the effective filing date of the claimed invention to a person having ordinary skill in the art to which the claimed invention pertains. Patentability shall not be negated by the manner in which the invention was made. Claim(s) 9 is/are rejected under 35 U.S.C. 103 as being unpatentable over Smith (US 2012/0245429 A1) in view of Penenberg (US 2006/0189848 A1). In regards to claim 9, Smith teaches the apparatus of claim 1. Smith teaches in Figure 7 that the batten (elongate member 140) is L-shaped (Figure 7 teaches the elongate member 140 having an angled structure resembling the shape of a capital letter “L”) such that the handle portion (portion of elongate member 140 external to tube 130 in use; shown in Figure 5; can be considered a “handle” inasmuch as it is capable of being manually grasped) is angled with respect to the reinforcing portion (portion of elongate member 140 positioned within tube 130 in use; see Figure 5; [0025] teaches “an elongate member 140 insertable into tube 130”); the handle portion (portion of elongate member 140 external to tube 130 in use; shown in Figure 5; can be considered a “handle” inasmuch as it is capable of being manually grasped) being substantially straight (as shown in Figure 7) and extending radially away from the longitudinal axis (Figure 7 teaches the portion of elongate member 140 external to tube 130 in use extending laterally away from the vertical axis of the device). Smith does not teach that the angle is perpendicular. However, Penenberg teaches in Figures 1 and 2A an analogous device in which the handle portion (surface support portion 14) is perpendicular to (as shown in Figures 1 and 2A) the reinforcing portion (site anchor portion 10). It would have been obvious to one having ordinary skill in the art before the effective filing of the present invention to modify the angle of Smith to be perpendicular as taught by Penenberg because this element is known to be a configuration “conventional” in the art, as Penenberg teaches in [0019]. Further, it would have been obvious to one having ordinary skill in the art before the effective filing of the present invention to provide the handle portion is perpendicular to the reinforcing portion, since it has been held that rearranging parts of an invention involves only routine skill in the art. In re Japikse, 86 USPQ 70. One having ordinary skill in the art before the effective filing of the present invention would find it obvious that the angle of the handle portion relative to the reinforcing portion could be modified to most comfortably and affectively accommodate the manual grip and manipulation of a particular user. Claim(s) 17 is/are rejected under 35 U.S.C. 103 as being unpatentable over Smith (US 2012/0245429 A1). In regards to claim 17, Smith teaches the apparatus of claim 1. Smith does not teach that the reinforcing portion and the handle portion of the batten have a width of one inch. However, it would have been obvious to one having ordinary skill in the art before the effective filing of the present invention to provide that the reinforcing portion and the handle portion of the batten have a width of one inch, since it has been held that where the general conditions of a claim are disclosed in the prior art, discovering the optimum or workable ranges involves only routine skill in the art. In re Aller, 105 USPQ 233. One having ordinary skill in the art before the effective filing of the present invention would find it obvious that the width of the reinforcing portion and the handle portion of the batten could be modified necessary to accommodate the size if a particular surgical incision and/or to most comfortably accommodate the manual grasp of a particular user. Conclusion Applicant's amendment necessitated the new ground(s) of rejection presented in this Office action. Accordingly, THIS ACTION IS MADE FINAL. See MPEP § 706.07(a). Applicant is reminded of the extension of time policy as set forth in 37 CFR 1.136(a). A shortened statutory period for reply to this final action is set to expire THREE MONTHS from the mailing date of this action. In the event a first reply is filed within TWO MONTHS of the mailing date of this final action and the advisory action is not mailed until after the end of the THREE-MONTH shortened statutory period, then the shortened statutory period will expire on the date the advisory action is mailed, and any nonprovisional extension fee (37 CFR 1.17(a)) pursuant to 37 CFR 1.136(a) will be calculated from the mailing date of the advisory action. In no event, however, will the statutory period for reply expire later than SIX MONTHS from the mailing date of this final action. Any inquiry concerning this communication or earlier communications from the examiner should be directed to VICTORIA H FISHER whose telephone number is (571)270-7033. The examiner can normally be reached M-TH 6:00AM-4:00PM EST. Examiner interviews are available via telephone, in-person, and video conferencing using a USPTO supplied web-based collaboration tool. To schedule an interview, applicant is encouraged to use the USPTO Automated Interview Request (AIR) at http://www.uspto.gov/interviewpractice. If attempts to reach the examiner by telephone are unsuccessful, the examiner’s supervisor, Rachael Bredefeld can be reached at (571) 270-5237. The fax phone number for the organization where this application or proceeding is assigned is 571-273-8300. Information regarding the status of published or unpublished applications may be obtained from Patent Center. Unpublished application information in Patent Center is available to registered users. To file and manage patent submissions in Patent Center, visit: https://patentcenter.uspto.gov. Visit https://www.uspto.gov/patents/apply/patent-center for more information about Patent Center and https://www.uspto.gov/patents/docx for information about filing in DOCX format. For additional questions, contact the Electronic Business Center (EBC) at 866-217-9197 (toll-free). If you would like assistance from a USPTO Customer Service Representative, call 800-786-9199 (IN USA OR CANADA) or 571-272-1000. /VICTORIA HICKS FISHER/Primary Examiner, Art Unit 3786 6/24/2026
Read full office action

Prosecution Timeline

Jan 16, 2024
Application Filed
Oct 27, 2025
Non-Final Rejection mailed — §102, §103, §112
Jan 27, 2026
Response Filed
Jun 26, 2026
Final Rejection mailed — §102, §103, §112 (current)

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Study what changed to get past this examiner. Based on 5 most recent grants.

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Prosecution Projections

3-4
Expected OA Rounds
41%
Grant Probability
79%
With Interview (+38.1%)
4y 2m (~1y 8m remaining)
Median Time to Grant
Moderate
PTA Risk
Based on 686 resolved cases by this examiner. Grant probability derived from career allowance rate.

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