FDA 510(k)

SMITH & NEPHEW FEMORAL HEADS

K-Number: K024340 · 2003-02-26

Decision Date2003-02-26

Product CodeJDI

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

SMITH & NEPHEW FEMORAL HEADS 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 2003-02-26 under 510(k) number K024340. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMITH & NEPHEW FEMORAL HEADS?

SMITH & NEPHEW FEMORAL HEADS is a medical device that received FDA 510(k) clearance on 2003-02-26. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K024340.

When did SMITH & NEPHEW FEMORAL HEADS receive FDA 510(k) clearance?

SMITH & NEPHEW FEMORAL HEADS received FDA 510(k) clearance on 2003-02-26, under 510(k) number K024340.

Who is the listed applicant for SMITH & NEPHEW FEMORAL HEADS?

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 SMITH & NEPHEW FEMORAL HEADS?

The FDA product code for SMITH & NEPHEW FEMORAL HEADS is JDI.

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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.