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FDA 510(k)

TRILOGY LONGEVITY CONSTRAINED LINER

K-Number: K071718 · 2007-07-13

ApplicantZimmer, Inc.
Decision Date2007-07-13
Product CodeKWZ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TRILOGY LONGEVITY CONSTRAINED LINER is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 2007-07-13 under 510(k) number K071718. 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 TRILOGY LONGEVITY CONSTRAINED LINER?

TRILOGY LONGEVITY CONSTRAINED LINER is a medical device that received FDA 510(k) clearance on 2007-07-13. The listed applicant is Zimmer, Inc.. The 510(k) number is K071718.

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

TRILOGY LONGEVITY CONSTRAINED LINER received FDA 510(k) clearance on 2007-07-13, under 510(k) number K071718.

Who is the listed applicant for TRILOGY LONGEVITY CONSTRAINED LINER?

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

What is the FDA product code for TRILOGY LONGEVITY CONSTRAINED LINER?

The FDA product code for TRILOGY LONGEVITY CONSTRAINED LINER is KWZ.

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Related Devices (Code: KWZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K241461Mpact Constrained LinerMedacta International S.A.K240639PINNACLETM Constrained Acetabular LinersDepuy Ireland UCK162641Smith & Nephew, Inc. R3™ Constrained LinerSmith & Nephew, Inc.K163497EXPRT™ Revision Hip System - EXPRT™ Hip Distal Stem, EXPRT™ Hip Standard Offset Proximal Body Implant, EXPRT™ Hip Lateral Offset Proximal Body Implant, EXPRT™ Hip Capture BoltEncore Medical L.P.K161610EXPRT Revision Hip SystemEncore Medical L.P.K122139SMITH & NEPHEW R3 CONSTRAINED LINERSSmith & Nephew, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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