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FDA 510(k)

TOTAL HIP FEMORAL HEAD - 12/14 TAPER

K-Number: K021673 · 2002-06-11

ApplicantSmith & Nephew, Inc.
Decision Date2002-06-11
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TOTAL HIP FEMORAL HEAD - 12/14 TAPER 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 2002-06-11 under 510(k) number K021673. 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 TOTAL HIP FEMORAL HEAD - 12/14 TAPER?

TOTAL HIP FEMORAL HEAD - 12/14 TAPER is a medical device that received FDA 510(k) clearance on 2002-06-11. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K021673.

When did TOTAL HIP FEMORAL HEAD - 12/14 TAPER receive FDA 510(k) clearance?

TOTAL HIP FEMORAL HEAD - 12/14 TAPER received FDA 510(k) clearance on 2002-06-11, under 510(k) number K021673.

Who is the listed applicant for TOTAL HIP FEMORAL HEAD - 12/14 TAPER?

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 TOTAL HIP FEMORAL HEAD - 12/14 TAPER?

The FDA product code for TOTAL HIP FEMORAL HEAD - 12/14 TAPER 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.

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