FDA 510(k)

SMITH & NEPHEW SUTURELOK, MODEL 7207321

K-Number: K000717 · 2000-03-30

Decision Date2000-03-30

Product CodeOCW

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

SMITH & NEPHEW SUTURELOK, MODEL 7207321 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 2000-03-30 under 510(k) number K000717. The device is classified under product code OCW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMITH & NEPHEW SUTURELOK, MODEL 7207321?

SMITH & NEPHEW SUTURELOK, MODEL 7207321 is a medical device that received FDA 510(k) clearance on 2000-03-30. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K000717.

When did SMITH & NEPHEW SUTURELOK, MODEL 7207321 receive FDA 510(k) clearance?

SMITH & NEPHEW SUTURELOK, MODEL 7207321 received FDA 510(k) clearance on 2000-03-30, under 510(k) number K000717.

Who is the listed applicant for SMITH & NEPHEW SUTURELOK, MODEL 7207321?

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 SMITH & NEPHEW SUTURELOK, MODEL 7207321?

The FDA product code for SMITH & NEPHEW SUTURELOK, MODEL 7207321 is OCW.

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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.