Prosecution Insights
Last updated: August 06, 2026
Application No. 18/485,875

VARIABLE EXPOSURE NEEDLE

Non-Final OA §102§103§112
Filed
Oct 12, 2023
Priority
Dec 07, 2022 — provisional 63/386,415
Examiner
PRICE, NATHAN R
Art Unit
3783
Tech Center
3700 — Mechanical Engineering & Manufacturing
Assignee
Boston Scientific Scimed Inc.
OA Round
1 (Non-Final)
53%
Grant Probability
Moderate
1-2
OA Rounds
1y 2m
Est. Remaining
92%
With Interview

Examiner Intelligence

Grants 53% of resolved cases
53%
Career Allowance Rate
269 granted / 510 resolved
-17.3% vs TC avg
Strong +40% interview lift
Without
With
+39.8%
Interview Lift
resolved cases with interview
Typical timeline
4y 0m
Avg Prosecution
22 currently pending
Career history
553
Total Applications
across all art units

Statute-Specific Performance

§101
1.5%
-38.5% vs TC avg
§103
41.8%
+1.8% vs TC avg
§102
27.7%
-12.3% vs TC avg
§112
21.6%
-18.4% vs TC avg
Black line = Tech Center average estimate • Based on career data from 510 resolved cases

Office Action

§102 §103 §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 . Response to Amendment This office action is responsive to the amendment filed on 11/5/25. As directed by the amendment: no claims have been amended, 1-15 and 25-35 have been cancelled, and no new claims have been added. Thus, claims 16-24 are presently pending in this application. Election/Restrictions Applicant’s election of Group I (claims 16-24) in the reply filed on 11/5/25 is acknowledged. Because applicant did not distinctly and specifically point out the supposed errors in the restriction requirement, the election has been treated as an election without traverse (MPEP § 818.01(a)). 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 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, it is unclear how the sharp distal end can be both covered via the access cannula, as recited in parent claim 16, and protrude distally from the access cannula, as recited in dependent claim 21; claim 21 is therefore indefinite. The following is a quotation of 35 U.S.C. 112(d): (d) REFERENCE IN DEPENDENT FORMS.—Subject to subsection (e), a claim in dependent form shall contain a reference to a claim previously set forth and then specify a further limitation of the subject matter claimed. A claim in dependent form shall be construed to incorporate by reference all the limitations of the claim to which it refers. The following is a quotation of pre-AIA 35 U.S.C. 112, fourth paragraph: Subject to the following paragraph [i.e., the fifth paragraph of pre-AIA 35 U.S.C. 112], a claim in dependent form shall contain a reference to a claim previously set forth and then specify a further limitation of the subject matter claimed. A claim in dependent form shall be construed to incorporate by reference all the limitations of the claim to which it refers. Claim 21 is rejected under 35 U.S.C. 112(d) or pre-AIA 35 U.S.C. 112, 4th paragraph, as being of improper dependent form for failing to further limit the subject matter of the claim upon which it depends, or for failing to include all the limitations of the claim upon which it depends. Claim 21, as worded, fails to include all the limitations of claim 16 on which it depends, and specifically fails to include the sharp distal end being covered via the access cannula as recited in claim 1, instead broadening the limitation so that the sharp distal end is not covered and protrudes distally. Applicant may cancel the claim(s), amend the claim(s) to place the claim(s) in proper dependent form, rewrite the claim(s) in independent form, or present a sufficient showing that the dependent claim(s) complies with the statutory requirements. 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) 16, 19, 20, 22, and 23 is/are rejected under 35 U.S.C. 102(a)(1) as being anticipated by Adams (US 2847995). Regarding claim 16, Adams discloses a system for accessing a biliary duct (system illustrated in fig. 5-8, fully capable of accessing a biliary duct via puncture with the tip as illustrated), comprising: an access cannula 41 extending along a longitudinal axis from a proximal end to a distal end (distal end toward sharp tip and proximal end toward hub) and including a channel 42 extending longitudinally therethrough, a distal portion of the access cannula including a laser cut pattern (pattern formed by elements 33, which are a product fully capable of formation via a laser cut pattern process of making that product) including a plurality of slots 43 extending through a wall thereof (see fig. 8; 43 are slots that extend through at least a portion of the wall diameter) so that the access cannula is movable between a biased non-compressed configuration (fig. 5, 6, or 8) and a compressed configuration (fig. 7), in which the access cannula is compressed along the longitudinal axis (see fig. 7); and a needle 47 extending longitudinally from a proximal end to a sharp distal end (see fig. 5-8), the needle housed within the channel of the access cannula (see fig. 5, 6, and 8) so that, when the access cannula is in the non-compressed configuration, the sharp distal end is covered via the access cannula (see fig. 5, 6, and 8) and, when the access cannula is in the compressed configuration, the sharp distal end is exposed to puncture a wall of one of an organ and a target duct (see fig. 7). Regarding claim 19, Adams discloses the laser cut pattern is selected to achieve a desired level of compressibility for the access cannula (desired compressibility achieved as illustrated in fig. 7), the desired level of compressibility including a compressive force required to move the access cannula from the non-compressed configuration toward the compressed configuration and length by which the access cannula is shortened when moved from the non-compressed configuration toward the compressed configuration (See fig. 5-8). Regarding claim 20, Adams discloses the desired level of compressibility achieved via the laser cut pattern is based on one of a number of slots per row, dimensions of each of the slots, a rotation angle between corresponding slots in adjacent rows, and a distance between rows (compressibility of 41 is achieved at least via the dimensions of slots and distance between rows as illustrated in fig. 5-8). Regarding claim 22, Adams discloses when the access cannula is moved from the non-compressed configuration to the compressed configuration, the access cannula is shortened via a distance corresponding to the sharp distal end of the needle (distance corresponding to the sharp tip of the needle is uncovered during transition from configuration to configuration as claimed, comparing fig. 5/6 to fig. 7). Regarding claim 23, Adams discloses a length of the sharp distal end of the needle that is exposed when the access cannula is in the compressed configuration is smaller than the target duct such to prevent a through and through puncture (structure of fig. 5-8 is fully capable of performing this claimed function, at least by compressing only to expose a desired length). 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. This application currently names joint inventors. In considering patentability of the claims the examiner presumes that the subject matter of the various claims was commonly owned as of the effective filing date of the claimed invention(s) absent any evidence to the contrary. Applicant is advised of the obligation under 37 CFR 1.56 to point out the inventor and effective filing dates of each claim that was not commonly owned as of the effective filing date of the later invention in order for the examiner to consider the applicability of 35 U.S.C. 102(b)(2)(C) for any potential 35 U.S.C. 102(a)(2) prior art against the later invention. Claim(s) 17 and 18 is/are rejected under 35 U.S.C. 103 as being unpatentable over Adams in view of Aramo (US 3134380). Regarding claims 17 and 18, Adams discloses the laser cut pattern includes a plurality of rows (each of 43 is one row), each row extending about a periphery of the access cannula (see fig. 8), each of the rows including at least one slot extending along a portion of the row (see fig. 8), wherein each row extends perpendicular to the longitudinal axis of the cannula (see fig. 5-8), except for specifically disclosing the rows extending through the wall such that the channel of the access cannula is open to and in communication with an exterior of the access cannula via the slots. However, Aramo teaches extending a portion of a slot in a compressible sleeve through the wall such that the access cannula is open to the exterior, via 31 (see fig. 6). It would have been obvious to one having ordinary skill in the art before the effective filing date of the claimed invention to extend at least a portion of each row of Adams through the wall such that the channel is open to the exterior, as taught by Aramo, for the purpose of providing sufficient structure to allow air to escape from the interior to accommodate the collapsing of the cannula (col. 1, ln. 67- col. 2, ln. 27). Claim(s) 21, as best understood, is/are rejected under 35 U.S.C. 103 as being unpatentable over Adams in view of Schwartz (US 3867937). Regarding claim 21, as best understood, Adams disloses the device as claimed, except for, in the non-compressed configuration, a distal-most tip of the needle protrudes distally of the distal end of the access cannula. However, Schwartz teaches extending a distal tip of a needle past the distal end of the access cannula in the non-compressed configuration (see fig. 1-2). It would have been obvious to one having ordinary skill in the art before the effective filing date of the claimed invention to modify Adams to extend the distal tip pas the distal end of the access cannula, as taught by Schwartz, for the purpose of providing sufficient structure to allow initial puncture/placement while protecting the majority of the needle with the collapsible sleeve. Claim(s) 24 is/are rejected under 35 U.S.C. 103 as being unpatentable over Adams in view of Prestidge et al. (US 20040193109). Regarding claim 24, Adams discloses the device as claimed, except for the access cannula formed of a nitinol hypotube. However, Prestidge et al. teaches forming a collapsible/expandable access cannula 17 from NiTi (see fig. 1-2; par. 0035-0037). It would have been obvious to one having ordinary skill in the art before the effective filing date of the claimed invention to modify the cannula of Adams to utilize a nitinol hypotube, as taught by Prestidge et al., for the purpose of providing sufficient structure for controlled extension/contraction of the cannula. Conclusion The prior art made of record and not relied upon is considered pertinent to applicant's disclosure: Yoon (US 5707362) – example of slots extending through the wall, but longitudinally Schondorff et al. (US 20210268179) – interchangeability of longitudinal/transverse slots Cabiri (US 20130304035) – transverse slots Any inquiry concerning this communication or earlier communications from the examiner should be directed to NATHAN R PRICE whose telephone number is (571)270-5421. The examiner can normally be reached Mon-Fri 8:00am-4:00pm Eastern time. 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, Michael Tsai can be reached at 571-270-5246. 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. /NATHAN R PRICE/Primary Examiner, Art Unit 3783
Read full office action

Prosecution Timeline

Oct 12, 2023
Application Filed
May 13, 2026
Non-Final Rejection mailed — §102, §103, §112 (current)

Precedent Cases

Applications granted by this same examiner with similar technology

Patent 12697422
A BREAST PUMP
3y 10m to grant Granted Aug 04, 2026
Patent 12691007
USER SELECTED CONFIDENCE LEVEL FOR IDENTIFICATION OF AN IMMINENT VACUUM SURGE DURING PHACOEMULSIFICATION
3y 7m to grant Granted Jul 28, 2026
Patent 12673069
INTRA-ARTICULAR NEEDLE PLACEMENT DEVICE AND METHOD OF USING
4y 0m to grant Granted Jul 07, 2026
Patent 12660998
OSCILLATING ENDOSCOPIC CATHETER FOR FALLOPIAN TUBE NAVIGATION
3y 4m to grant Granted Jun 23, 2026
Patent 12599365
STABILIZING TRANSNASAL BALLOON SHEATH
4y 6m to grant Granted Apr 14, 2026
Study what changed to get past this examiner. Based on 5 most recent grants.

Strategy Recommendation AI-generated — please review before filing

Get a prosecution strategy drawn from examiner precedents, rejection analysis, and claim mapping.
Typically takes 5-10 seconds — AI-generated, attorney review required before filing

Prosecution Projections

1-2
Expected OA Rounds
53%
Grant Probability
92%
With Interview (+39.8%)
4y 0m (~1y 2m remaining)
Median Time to Grant
Low
PTA Risk
Based on 510 resolved cases by this examiner. Grant probability derived from career allowance 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