Prosecution Insights
Last updated: July 17, 2026
Application No. 18/204,802

MEDICAL DEVICE FOR STIMULATING NEURONS OF A PATIENT TO SUPPRESS A PATHOLOGICALLY SYNCHRONOUS NEURONAL ACTIVITY

Non-Final OA §103§112
Filed
Sep 06, 2023
Priority
Dec 02, 2020 — provisional 63/120,229 +1 more
Examiner
OJO, OYESOLA C
Art Unit
3799
Tech Center
3700 — Mechanical Engineering & Manufacturing
Assignee
Gretap AG
OA Round
1 (Non-Final)
82%
Grant Probability
Favorable
1-2
OA Rounds
0m
Est. Remaining
94%
With Interview

Examiner Intelligence

Grants 82% — above average
82%
Career Allowance Rate
604 granted / 732 resolved
+12.5% vs TC avg
Moderate +11% lift
Without
With
+11.1%
Interview Lift
resolved cases with interview
Fast prosecutor
2y 1m
Avg Prosecution
14 currently pending
Career history
745
Total Applications
across all art units

Statute-Specific Performance

§101
0.3%
-39.7% vs TC avg
§103
91.6%
+51.6% vs TC avg
§102
6.0%
-34.0% vs TC avg
§112
0.7%
-39.3% vs TC avg
Black line = Tech Center average estimate • Based on career data from 732 resolved cases

Office Action

§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 . Status of Claims Claims 1-5 and 15 are rejected Claims 6-14, 16-20 are objected to 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 15 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 15 merely recites ‘a use’ without any active, positive steps delimiting how this use is actually practiced. This renders the claim indefinite. Claim Rejections - 35 USC § 103 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 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. The factual inquiries for establishing a background for determining obviousness under 35 U.S.C. 103 are summarized as follows: 1. Determining the scope and contents of the prior art. 2. Ascertaining the differences between the prior art and the claims at issue. 3. Resolving the level of ordinary skill in the pertinent art. 4. Considering objective evidence present in the application indicating obviousness or nonobviousness. Claim(s) 1-5 and 15 is/are rejected under 35 U.S.C. 103 as being unpatentable over Baker et al (US PUB 20200129760, hereinafter Baker). Regarding Claim 1, Baker discloses a medical device for stimulating neurons of a patient to suppress a pathologically synchronous activity of the neurons (e.g. a tinnitus treatment device 100), (see [0024], and figures 1-3), comprising: a stimulation unit configured for selectively generating acoustic stimuli to be administered to the patient (e.g. earbuds 160, 170 selectively apply stimuli to the user) and a control unit (e.g. a controller) for actuating the stimulation unit to generate a plurality of stimuli of different frequencies (e.g. plurality of tinnitus therapy sound templates that are based on different frequencies), (see [0047]-[0048], [0058]-[0059] and [0066], also figure 3-4), wherein the control unit is configured to determine a target frequency range (e.g. specific frequency ranges) within a hearing range of the patient in dependence on an auditory perception of the patient (see figure 5B); and to select the plurality of stimuli such that the frequencies of the plurality of stimuli are within the target frequency range (e.g. in step 560, plurality of stimuli having frequency within the target frequency range are selected), (see Baker, [0073]-[0075] and [0087]-[0089], also figures 5B and 6). Baker does not explicitly disclose that the frequencies of the selected plurality stimuli correspond to tone frequencies of a musical scale spanning at least one octave. However, Middlebrooks in the same field of endeavor teaches that tit is well known in the art to select plurality of stimuli having frequencies corresponding to tone frequencies of a musical scale spanning at least one octave as set forth in [0036], and figure 3. Therefore, it would have been obvious to any person having an ordinary skill in the art to incorporate selecting plurality of stimuli with frequencies spanning at least one octave as taught by Middlebrooks in the teachings of Baker in order to effectively suppress high pitched hearing problems such as tinnitus in the patient. Regarding Claim 2, Baker as modified by Middlebrooks discloses the medical device according to claim 1, wherein the control unit is configured to determine the target frequency range (e.g. specific tinnitus therapy sounds) in dependence on a subjective evaluation of the auditory perception of the patient (see Baker, [0023] and figure 3). Regarding Claim 3, Baker as modified by Middlebrooks discloses the medical device according to claim 1, wherein the control unit is configured to determine the target frequency range in dependence on an evaluation of at least one frequency-dependent characteristic of the auditory perception of the patient (see Baker, [0023] and figure 3). Regarding Claim 4, Baker as modified by Middlebrooks discloses the medical device according to claim 1, wherein the control unit is configured to determine the target frequency in dependence on at least one of an audiogram determination procedure, a psychoacoustic tinnitus spectrum determination procedure, a procedure for determining auditory hallucinations, a similarity measure procedure, or a procedure for determining pleasantness or unpleasantness of different tones experienced by the patient (see Baker, [0023] and figure 3). Regarding Claim 5, Baker as modified by Middlebrooks discloses the medical device according to claim 1, wherein the musical scale comprises a pitch pattern consisting of a plurality of pitches per octave (see Baker, [0066] and [0073], also figure 3). Regarding Claim 15, Baker as modified by Middlebrooks discloses a method, comprising using the medical device according to claim 1 to treat a pathologically synchronous activity of neurons of the patient (see Baker, [0022] and [0112]) Allowable Subject Matter Claims 6-14, 16-20 are objected to as being dependent upon a rejected base claim, but would be allowable if rewritten in independent form including all of the limitations of the base claim and any intervening claims. Conclusion The prior art made of record provided on PTO 892 and not relied upon is considered pertinent to applicant's disclosure. Any inquiry concerning this communication or earlier communications from the examiner should be directed to OYESOLA C OJO whose telephone number is (571)272-0848. The examiner can normally be reached Monday through Friday 8:00am to 4:00pm Central 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, Vivian Chin can be reached at 571-272-7840. 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. /OYESOLA C OJO/Primary Examiner, Art Unit 2695
Read full office action

Prosecution Timeline

Sep 06, 2023
Application Filed
Sep 06, 2023
Response after Non-Final Action
May 14, 2026
Non-Final Rejection mailed — §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

1-2
Expected OA Rounds
82%
Grant Probability
94%
With Interview (+11.1%)
2y 1m (~0m remaining)
Median Time to Grant
Low
PTA Risk
Based on 732 resolved cases by this examiner. Grant probability derived from career allowance rate.

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