FDA 510(k)

REFLECTION CONSTRAINED LINER

K-Number: K021803 · 2002-12-19

Decision Date2002-12-19

Product CodeKWZ

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

REFLECTION CONSTRAINED LINER 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 2002-12-19 under 510(k) number K021803. The device is classified under product code KWZ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REFLECTION CONSTRAINED LINER?

REFLECTION CONSTRAINED LINER is a medical device that received FDA 510(k) clearance on 2002-12-19. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K021803.

When did REFLECTION CONSTRAINED LINER receive FDA 510(k) clearance?

REFLECTION CONSTRAINED LINER received FDA 510(k) clearance on 2002-12-19, under 510(k) number K021803.

Who is the listed applicant for REFLECTION CONSTRAINED LINER?

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 REFLECTION CONSTRAINED LINER?

The FDA product code for REFLECTION CONSTRAINED LINER is KWZ.

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Related Devices (Code: KWZ)

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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.