Prosecution Insights
Last updated: April 19, 2026
Application No. 18/124,623

MEDICAL APPARATUS AND POSITIONING METHOD FOR TREATMENT INSTRUMENT

Final Rejection §102§112
Filed
Mar 22, 2023
Examiner
HENDERSON, RYAN N
Art Unit
3795
Tech Center
3700 — Mechanical Engineering & Manufacturing
Assignee
Olympus Medical Systems Corp.
OA Round
2 (Final)
64%
Grant Probability
Moderate
3-4
OA Rounds
4y 3m
To Grant
82%
With Interview

Examiner Intelligence

Grants 64% of resolved cases
64%
Career Allow Rate
514 granted / 807 resolved
-6.3% vs TC avg
Strong +18% interview lift
Without
With
+17.9%
Interview Lift
resolved cases with interview
Typical timeline
4y 3m
Avg Prosecution
46 currently pending
Career history
853
Total Applications
across all art units

Statute-Specific Performance

§101
0.5%
-39.5% vs TC avg
§103
34.6%
-5.4% vs TC avg
§102
33.5%
-6.5% vs TC avg
§112
28.0%
-12.0% vs TC avg
Black line = Tech Center average estimate • Based on career data from 807 resolved cases

Office Action

§102 §112
DETAILED ACTION 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 . Notice of Amendment The Amendment filed 1/20/2026 has been entered. Claims 1-3, 5-21 are pending in the application with claims 1, 3, 5, 7, 9, 10, 14, 18 and 19 amended, claim 5 withdrawn, claim 4 cancelled, and claim 21 newly added. Claim Rejections - 35 USC § 112 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 20 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. Claim 20 recites “a first gear provided an in inner circumferential surface of the operation slider” in Line 3, wherein it’s unclear how the first gear is disposed on the operation slider since Fig. 4 illustrates the operation slider as element (28) which has no gear on an inner circumferential surface thereof. However, the operation slider (28) is meant to engage operation knob (27) which does have a gear disposed on an inner circumferential surface thereof. Appropriate correction is required. Claim Rejections - 35 USC § 102 In the event the determination of the status of the application as subject to AIA 35 U.S.C. 102 and 103 (or as subject to pre-AIA 35 U.S.C. 102 and 103) is incorrect, any correction of the statutory basis (i.e., changing from AIA to pre-AIA ) for the rejection will not be considered a new ground of rejection if the prior art relied upon, and the rationale supporting the rejection, would be the same under either status. 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. Claims 1, 2, 8-19 and 21 are rejected under 35 U.S.C. 102(a)(1) as being anticipated by Yamane (JP 2009-183389A). In regard to claim 1, Yamane discloses a medical apparatus (1, Fig. 1), comprising: an insertion section (2, 3); and a treatment instrument channel (35) located in the insertion section, the treatment instrument channel including a coil (32) formed by a wound element wire (Fig. 3), wherein the coil forms an inner diameter surface of the treatment instrument channel (Figs. 3-5), wherein the treatment instrument channel is configured to be deformed by an operational force (Fig. 5), and wherein in response to the operational force transmitted to the treatment instrument channel, the coil changes a cross-sectional area of the treatment instrument channel in a direction intersecting an axis of the treatment instrument channel (Figs. 4-5, via axial movement of the channel operation member). In regard to claim 2, Yamane teaches wherein the direction intersecting the axis is a perpendicular to the axis (Fig. 5). In regard to claim 8, Yamane teaches further comprising: an illumination unit (10) configured to illuminate an operation site (Fig. 2), and an image pickup sensor (11) configured to obtain an image of the operation site (Fig. 2). In regard to claim 9, Yamane discloses a medical apparatus (1, Fig. 1), comprising: an insertion section (2, 3); a treatment instrument channel (35) located in the insertion section (Fig. 3); a coil (32) formed by a wound element wire and located in at least a part of the treatment instrument channel (Fig. 3); and a channel operation member (32) coupled to the treatment instrument channel for transmitting an operational force to the coil (Figs. 4-5), wherein the coil forms an inner diameter surface of the treatment instrument channel (Figs. 3-5), wherein, in response to the operational force transmitted to the coil by the channel operation member, the coil changes a cross-sectional area of an inside of the treatment instrument channel in a direction intersecting an axis of the treatment instrument channel (Figs. 4-5, via axial movement of the channel operation member). In regard to claim 10, Yamane discloses a method for positioning a treatment instrument using the medical apparatus (1, Fig. 1) according to claim 1(see rejection of Claim 1), the method comprising: inserting the treatment instrument to a predetermined position of the treatment instrument channel; and changing the cross-sectional area of the treatment instrument channel in the direction intersecting the axis of the treatment instrument channel (the coil (32) is biased to a closed state to form a seal whether an instrument is within the channel or not and further operation of member (34) enables transitioning between the open and closed states to compress/expand the coil). In regard to claim 11, Yamane teaches wherein changing the cross-sectional area of the treatment instrument channel includes reducing a diameter partway along a longitudinal axis of the treatment instrument channel (Fig. 5). In regard to claim 12, Yamane teaches wherein changing the cross-sectional area of the treatment instrument channel includes reducing the cross-sectional area of at least a part of the treatment instrument channel (Fig. 5). In regard to claim 13, Yamane teaches wherein the operational force is a force in a twisting direction or in a towing direction (via axial displacement of member (34)). In regard to claim 14, Yamane teaches wherein the method further comprises moving a first part of the treatment instrument channel relative to a second part of the treatment instrument channel around the axis of the treatment instrument channel to transmit the operational force to the second part of the treatment instrument channel (Fig. 5, via the middle section of the coil (32) which engages the bulge is compressed relative to the ends of the coil). In regard to claim 15, Yamane teaches wherein the treatment instrument includes an end effector, and wherein the predetermined position is a position where the end effector is located distally relative to a position where the cross-sectional area is changed (Par. 14, wherein the distal end of the forceps would be positioned distal to the compressed area of the coil since the coil is disposed at a proximal end of the channel). In regard to claim 16, Yamane teaches wherein the medical apparatus further comprises an image pickup sensor (11) having a field of view, wherein the image pickup sensor is located at a distal end of the insertion section, wherein the treatment instrument includes an end effector, and wherein the predetermined position is a position where the end effector is located within the field of view (the coil can be compressed about the forceps shaft while the end effector is disposed within a field of view of the image pickup sensor since the instrument channel opens adjacent a field of view of the image sensor). In regard to claim 17, Yamane teaches wherein the channel operation member is a ring (Figs. 4-5). In regard to claim 18, Yamane teaches further comprising: an operation section (2), wherein the treatment instrument channel extends from a proximal end located in the operation section to a distal end located in the insertion section (Figs. 1,3), wherein the treatment instrument channel includes a channel operation member (34) coupled to the coil for transmitting the operational force to the coil (Figs. 4-5), and wherein, in response to the operational force transmitted to the coil by the channel operation member, the coil is configured to deform to change the cross-sectional area of the treatment instrument channel in the direction intersecting the axis (via axial displacement of the channel operation member (34), Figs. 4-5). In regard to claim 19, Yamane teaches wherein the coil is configured to deform to change the cross-sectional area of the treatment instrument channel, and wherein the deformed second part coil has a tapered shape (Fig. 5). In regard to claim 21, Yamane teaches wherein the treatment instrument channel further includes an outer skin (31) that covers an outer circumference of the coil (Fig. 4). Claims 1, 3 and 6 are rejected under 35 U.S.C. 102(a)(1) as being anticipated by Kubokawa (JPS5636935A). In regard to claim 1, Kubokawa discloses a medical apparatus (1, Figs. 1, 8), comprising: an insertion section (3); and a treatment instrument channel located in the insertion section (via channel extending through an inner diameter of the pipe (4)), the treatment instrument channel including a coil (38) formed by a wound element wire (via spiral pipe (38), Fig. 8), wherein the coil forms an inner diameter surface of the treatment instrument channel (Fig. 8, Par. 2), wherein the treatment instrument channel is configured to be deformed by an operational force, and wherein in response to the operational force transmitted to the treatment instrument channel, the coil changes a cross-sectional area of the treatment instrument channel in a direction intersecting an axis of the treatment instrument channel (via rotation of operation ring (17) the degree of compression of the spiral pipe (38) is adjusted, Fig. 8). In regard to claim 3, Kubokawa teaches wherein the treatment instrument channel further includes a channel operation member (17) coupled to the coil for transmitting the operational force to the coil (Fig. 8, Par. 2), wherein the channel operation member is rotatable relative to the treatment instrument channel around the axis (Fig. 8, Par. 2), and wherein a rotation of the channel operation member relative to the treatment instrument channel around the axis transmits the operational force to the treatment instrument channel (Fig. 8, Par. 2). In regard to claim 6, Kubokawa teaches further comprising a lock (via member (20) which is fixed/locked to the sliding cylinder (15), Fig. 8, Par. 2). Claims 1 and 7 are rejected under 35 U.S.C. 102(a)(1) as being anticipated by Miller (US Patent Application Publication No. 2023/0016459). In regard to claim 1, Miller discloses a medical apparatus (150, Fig. 2), comprising: an insertion section (151, Fig. 1); and a treatment instrument channel (34,234) located in the insertion section (Fig. 4B), the treatment instrument channel including a coil formed by a wound element wire (Par. 91 teaches the channel extension (234) can take the form of a coil), wherein the coil forms an inner diameter surface of the treatment instrument channel (channel extension (234), which is formed by the coil forms an inner diameter surface of the channel, Figs. 17A-17B), wherein the treatment instrument channel is configured to be deformed by an operational force, and wherein in response to the operational force transmitted to the treatment instrument channel, the coil changes a cross-sectional area of the treatment instrument channel in a direction intersecting an axis of the treatment instrument channel (tilting of the channel extension (234) causes a compressive force within the channel extension, thereby locking an instrument within the channel, Par. 93, Figs. 17A-17B). In regard to claim 7, Miller teaches further comprising a treatment instrument insertable into the treatment instrument channel, wherein the insertion section includes: a distal end portion (152) including an opening for leading out the treatment instrument inserted through the treatment instrument channel (Fig. 2), a bending section (distal section of shaft (151)) provided at a proximal end of the distal end portion (Fig. 2), and a flexible tube section (proximal section of shaft (151)) provided at a proximal end of the bending section (Fig. 2), and wherein the coil is provided distally relative to the flexible tube section and deforms to change the cross-sectional area of the treatment instrument channel (the coil is disposed within the distal end portion of the shaft, Figs. 2, 4B). Response to Arguments Applicant’s arguments with respect to claims 1-3, 6-21 have been considered but are moot because the new ground of rejection does not rely on any reference applied in the prior rejection of record for any teaching or matter specifically challenged in the argument. 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 RYAN N HENDERSON whose telephone number is (571)270-1430. The examiner can normally be reached Monday-Friday 6am-5pm (PST). 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, Anhtuan Nguyen can be reached at 571-272-4963. 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. /RYAN N HENDERSON/Primary Examiner, Art Unit 3795 March 15, 2026
Read full office action

Prosecution Timeline

Mar 22, 2023
Application Filed
Nov 01, 2025
Non-Final Rejection — §102, §112
Jan 20, 2026
Response Filed
Mar 15, 2026
Final Rejection — §102, §112 (current)

Precedent Cases

Applications granted by this same examiner with similar technology

Patent 12599298
SYSTEMS AND METHODS FOR DETECTING PHYSICAL CONTACT OF A SURGICAL INSTRUMENT WITH PATIENT TISSUE
2y 5m to grant Granted Apr 14, 2026
Patent 12588804
ENDOSCOPE BENDING SECTION
2y 5m to grant Granted Mar 31, 2026
Patent 12543931
ENDOSCOPE CONTROL UNIT WITH BRAKING SYSTEM
2y 5m to grant Granted Feb 10, 2026
Patent 12543928
ELEVATOR FOR DIRECTING MEDICAL TOOL
2y 5m to grant Granted Feb 10, 2026
Patent 12539019
A HANDLE FOR AN ENDOSCOPE
2y 5m to grant Granted Feb 03, 2026
Study what changed to get past this examiner. Based on 5 most recent grants.

AI Strategy Recommendation

Get an AI-powered prosecution strategy using examiner precedents, rejection analysis, and claim mapping.
Powered by AI — typically takes 5-10 seconds

Prosecution Projections

3-4
Expected OA Rounds
64%
Grant Probability
82%
With Interview (+17.9%)
4y 3m
Median Time to Grant
Moderate
PTA Risk
Based on 807 resolved cases by this examiner. Grant probability derived from career allow rate.

Sign in with your work email

Enter your email to receive a magic link. No password needed.

Personal email addresses (Gmail, Yahoo, etc.) are not accepted.

Free tier: 3 strategy analyses per month