FDA 510(k)

CONTOUR HA COATED RECONSTRUCTION RING

K-Number: K040680 · 2004-06-14

Decision Date2004-06-14

Product CodeMEH

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

CONTOUR HA COATED RECONSTRUCTION RING 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 2004-06-14 under 510(k) number K040680. The device is classified under product code MEH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTOUR HA COATED RECONSTRUCTION RING?

CONTOUR HA COATED RECONSTRUCTION RING is a medical device that received FDA 510(k) clearance on 2004-06-14. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K040680.

When did CONTOUR HA COATED RECONSTRUCTION RING receive FDA 510(k) clearance?

CONTOUR HA COATED RECONSTRUCTION RING received FDA 510(k) clearance on 2004-06-14, under 510(k) number K040680.

Who is the listed applicant for CONTOUR HA COATED RECONSTRUCTION RING?

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 CONTOUR HA COATED RECONSTRUCTION RING?

The FDA product code for CONTOUR HA COATED RECONSTRUCTION RING is MEH.

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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.