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FDA 510(k)

Smith & Nephew, Inc. ANTHOLOGY™ AFIT Hip Stem

K-Number: K172684 · 2017-10-03

ApplicantSmith & Nephew, Inc.
Decision Date2017-10-03
Product CodeLPH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Smith & Nephew, Inc. ANTHOLOGY™ AFIT Hip Stem is a medical device manufactured by Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2017-10-03 under approval number K172684. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Smith & Nephew, Inc. ANTHOLOGY™ AFIT Hip Stem?

Smith & Nephew, Inc. ANTHOLOGY™ AFIT Hip Stem is a medical device that received FDA 510(k) clearance on 2017-10-03. It is manufactured by Smith & Nephew, Inc.. The 510(k) number is K172684.

When was Smith & Nephew, Inc. ANTHOLOGY™ AFIT Hip Stem approved by the FDA?

Smith & Nephew, Inc. ANTHOLOGY™ AFIT Hip Stem received FDA 510(k) clearance on 2017-10-03, under approval number K172684.

What company makes Smith & Nephew, Inc. ANTHOLOGY™ AFIT Hip Stem?

Smith & Nephew, Inc. ANTHOLOGY™ AFIT Hip Stem is manufactured by Smith & Nephew, Inc..

What is the FDA product code for Smith & Nephew, Inc. ANTHOLOGY™ AFIT Hip Stem?

The FDA product code for Smith & Nephew, Inc. ANTHOLOGY™ AFIT Hip Stem is LPH.

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Related Devices (Code: LPH)

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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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