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FDA 510(k)

Forcyte Autograft Harvest Kit

K-Number: K243407 · 2025-07-29

ApplicantForcyte Medical, LLC
Decision Date2025-07-29
Product CodeKNW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Forcyte Autograft Harvest Kit is the device name listed in this FDA 510(k) record. The listed applicant is Forcyte Medical, LLC. It received FDA 510(k) clearance on 2025-07-29 under 510(k) number K243407. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Forcyte Autograft Harvest Kit?

Forcyte Autograft Harvest Kit is a medical device that received FDA 510(k) clearance on 2025-07-29. The listed applicant is Forcyte Medical, LLC. The 510(k) number is K243407.

When did Forcyte Autograft Harvest Kit receive FDA 510(k) clearance?

Forcyte Autograft Harvest Kit received FDA 510(k) clearance on 2025-07-29, under 510(k) number K243407.

Who is the listed applicant for Forcyte Autograft Harvest Kit?

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

What is the FDA product code for Forcyte Autograft Harvest Kit?

The FDA product code for Forcyte Autograft Harvest Kit is KNW.

Related Devices (Code: KNW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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