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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 a medical device manufactured by Kneevoice, Inc.. It received FDA 510(k) clearance on 2026-02-06 under approval 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. It is manufactured by Kneevoice, Inc.. The 510(k) number is K252076.

When was Kneevoice Cartilage Evaluation System (750-3600-001) approved by the FDA?

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

What company makes Kneevoice Cartilage Evaluation System (750-3600-001)?

Kneevoice Cartilage Evaluation System (750-3600-001) is manufactured by Kneevoice, Inc..

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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Related PubMed Literature

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Official Source

View on FDA Database →

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

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