FDA 510(k)

SYNERGY CEMENTED HIP STEM

K-Number: K990369 · 1999-03-12

Decision Date1999-03-12

Product CodeJDI

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

SYNERGY CEMENTED 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 1999-03-12 under 510(k) number K990369. 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 SYNERGY CEMENTED HIP STEM?

SYNERGY CEMENTED HIP STEM is a medical device that received FDA 510(k) clearance on 1999-03-12. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K990369.

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

SYNERGY CEMENTED HIP STEM received FDA 510(k) clearance on 1999-03-12, under 510(k) number K990369.

Who is the listed applicant for SYNERGY CEMENTED 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 SYNERGY CEMENTED HIP STEM?

The FDA product code for SYNERGY CEMENTED 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.