FDA 510(k)

BARD CONTOUR LINK S.K.I. KNEE SYS

K-Number: K820002 · 1982-05-27

Decision Date1982-05-27

Product CodeHRY

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

BARD CONTOUR LINK S.K.I. KNEE SYS is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1982-05-27 under 510(k) number K820002. The device is classified under product code HRY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD CONTOUR LINK S.K.I. KNEE SYS?

BARD CONTOUR LINK S.K.I. KNEE SYS is a medical device that received FDA 510(k) clearance on 1982-05-27. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K820002.

When did BARD CONTOUR LINK S.K.I. KNEE SYS receive FDA 510(k) clearance?

BARD CONTOUR LINK S.K.I. KNEE SYS received FDA 510(k) clearance on 1982-05-27, under 510(k) number K820002.

Who is the listed applicant for BARD CONTOUR LINK S.K.I. KNEE SYS?

The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BARD CONTOUR LINK S.K.I. KNEE SYS?

The FDA product code for BARD CONTOUR LINK S.K.I. KNEE SYS is HRY.

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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.