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FDA 510(k)

EMPHASYS Femoral Stems

K-Number: K233233 · 2023-10-11

Decision Date2023-10-11
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

EMPHASYS Femoral Stems is a medical device manufactured by Depuy Ireland UC. It received FDA 510(k) clearance on 2023-10-11 under approval number K233233. 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 EMPHASYS Femoral Stems?

EMPHASYS Femoral Stems is a medical device that received FDA 510(k) clearance on 2023-10-11. It is manufactured by Depuy Ireland UC. The 510(k) number is K233233.

When was EMPHASYS Femoral Stems approved by the FDA?

EMPHASYS Femoral Stems received FDA 510(k) clearance on 2023-10-11, under approval number K233233.

What company makes EMPHASYS Femoral Stems?

EMPHASYS Femoral Stems is manufactured by Depuy Ireland UC.

What is the FDA product code for EMPHASYS Femoral Stems?

The FDA product code for EMPHASYS Femoral Stems is LZO.

Other Devices by Depuy Ireland UC

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Related Devices (Code: LZO)

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.