FDA 510(k)

ANTHOLOGY HIP STEM

K-Number: K052792 · 2005-10-07

Decision Date2005-10-07

Product CodeJDI

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

ANTHOLOGY HIP STEM 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 2005-10-07 under 510(k) number K052792. 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 ANTHOLOGY HIP STEM?

ANTHOLOGY HIP STEM is a medical device that received FDA 510(k) clearance on 2005-10-07. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K052792.

When did ANTHOLOGY HIP STEM receive FDA 510(k) clearance?

ANTHOLOGY HIP STEM received FDA 510(k) clearance on 2005-10-07, under 510(k) number K052792.

Who is the listed applicant for ANTHOLOGY HIP STEM?

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 ANTHOLOGY HIP STEM?

The FDA product code for ANTHOLOGY HIP STEM is JDI.

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Related Devices (Code: 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.