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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 a medical device manufactured by Forcyte Medical, LLC. It received FDA 510(k) clearance on 2025-07-29 under approval 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. It is manufactured by Forcyte Medical, LLC. The 510(k) number is K243407.

When was Forcyte Autograft Harvest Kit approved by the FDA?

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

What company makes Forcyte Autograft Harvest Kit?

Forcyte Autograft Harvest Kit is manufactured by Forcyte Medical, LLC.

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

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

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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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