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FDA 510(k)

Cellbrick Knee Spacer

K-Number: K243024 · 2024-12-20

Decision Date2024-12-20
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Cellbrick Knee Spacer is a medical device manufactured by United Orthopedic Corporation. It received FDA 510(k) clearance on 2024-12-20 under approval number K243024. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Cellbrick Knee Spacer?

Cellbrick Knee Spacer is a medical device that received FDA 510(k) clearance on 2024-12-20. It is manufactured by United Orthopedic Corporation. The 510(k) number is K243024.

When was Cellbrick Knee Spacer approved by the FDA?

Cellbrick Knee Spacer received FDA 510(k) clearance on 2024-12-20, under approval number K243024.

What company makes Cellbrick Knee Spacer?

Cellbrick Knee Spacer is manufactured by United Orthopedic Corporation.

What is the FDA product code for Cellbrick Knee Spacer?

The FDA product code for Cellbrick Knee Spacer is JWH.

Other Devices by United Orthopedic Corporation

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Related Devices (Code: JWH)

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.