FDA 510(k)

TAPER OXINIUM FEMORAL HEAD

K-Number: K110101 · 2011-04-11

Decision Date2011-04-11

Product CodeLZO

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

TAPER OXINIUM FEMORAL HEAD is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2011-04-11 under 510(k) number K110101. 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 TAPER OXINIUM FEMORAL HEAD?

TAPER OXINIUM FEMORAL HEAD is a medical device that received FDA 510(k) clearance on 2011-04-11. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K110101.

When did TAPER OXINIUM FEMORAL HEAD receive FDA 510(k) clearance?

TAPER OXINIUM FEMORAL HEAD received FDA 510(k) clearance on 2011-04-11, under 510(k) number K110101.

Who is the listed applicant for TAPER OXINIUM FEMORAL HEAD?

The FDA 510(k) record lists Smith & Nephew, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TAPER OXINIUM FEMORAL HEAD?

The FDA product code for TAPER OXINIUM FEMORAL HEAD is LZO.

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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.