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FDA 510(k)

Conformity Stem Extension Line, #0

K-Number: K243466 · 2025-01-06

Decision Date2025-01-06
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Conformity Stem Extension Line, #0 is a medical device manufactured by United Orthopedic Corporation. It received FDA 510(k) clearance on 2025-01-06 under approval number K243466. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Conformity Stem Extension Line, #0?

Conformity Stem Extension Line, #0 is a medical device that received FDA 510(k) clearance on 2025-01-06. It is manufactured by United Orthopedic Corporation. The 510(k) number is K243466.

When was Conformity Stem Extension Line, #0 approved by the FDA?

Conformity Stem Extension Line, #0 received FDA 510(k) clearance on 2025-01-06, under approval number K243466.

What company makes Conformity Stem Extension Line, #0?

Conformity Stem Extension Line, #0 is manufactured by United Orthopedic Corporation.

What is the FDA product code for Conformity Stem Extension Line, #0?

The FDA product code for Conformity Stem Extension Line, #0 is LZO.

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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.