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FDA 510(k)

Kneevoice Cartilage Evaluation System (750-3600-001)

K-Number: K252076 · 2026-02-06

ApplicantKneevoice, Inc.
Decision Date2026-02-06
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Kneevoice Cartilage Evaluation System (750-3600-001) is the device name listed in this FDA 510(k) record. The listed applicant is Kneevoice, Inc.. It received FDA 510(k) clearance on 2026-02-06 under 510(k) number K252076. The device is classified under product code DQD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Kneevoice Cartilage Evaluation System (750-3600-001)?

Kneevoice Cartilage Evaluation System (750-3600-001) is a medical device that received FDA 510(k) clearance on 2026-02-06. The listed applicant is Kneevoice, Inc.. The 510(k) number is K252076.

When did Kneevoice Cartilage Evaluation System (750-3600-001) receive FDA 510(k) clearance?

Kneevoice Cartilage Evaluation System (750-3600-001) received FDA 510(k) clearance on 2026-02-06, under 510(k) number K252076.

Who is the listed applicant for Kneevoice Cartilage Evaluation System (750-3600-001)?

The FDA 510(k) record lists Kneevoice, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Kneevoice Cartilage Evaluation System (750-3600-001)?

The FDA product code for Kneevoice Cartilage Evaluation System (750-3600-001) is DQD.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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