FDA 510(k)

TRILOGY ACETABULAR SYSTEM LARGE HEAD LINER, MODEL 6353

K-Number: K002960 · 2000-12-11

Decision Date2000-12-11

Product CodeLPH

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

TRILOGY ACETABULAR SYSTEM LARGE HEAD LINER, MODEL 6353 is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 2000-12-11 under 510(k) number K002960. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRILOGY ACETABULAR SYSTEM LARGE HEAD LINER, MODEL 6353?

TRILOGY ACETABULAR SYSTEM LARGE HEAD LINER, MODEL 6353 is a medical device that received FDA 510(k) clearance on 2000-12-11. The listed applicant is Zimmer, Inc.. The 510(k) number is K002960.

When did TRILOGY ACETABULAR SYSTEM LARGE HEAD LINER, MODEL 6353 receive FDA 510(k) clearance?

TRILOGY ACETABULAR SYSTEM LARGE HEAD LINER, MODEL 6353 received FDA 510(k) clearance on 2000-12-11, under 510(k) number K002960.

Who is the listed applicant for TRILOGY ACETABULAR SYSTEM LARGE HEAD LINER, MODEL 6353?

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 ACETABULAR SYSTEM LARGE HEAD LINER, MODEL 6353?

The FDA product code for TRILOGY ACETABULAR SYSTEM LARGE HEAD LINER, MODEL 6353 is LPH.

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Related Devices (Code: LPH)

K261453G7® Acetabular SystemZimmer Biomet K253630Mpact 3D Metal FoamMedacta International S.A.K254043TRIVANCE™ Hip StemGlobus Medical, Inc.K261624Omnifit® 20° Series I Insert;Omnifit® Crossfire® 10° Series II Insert; Constrained Acetabular Insert; Trident® Crossfire® 0° Polyethylene Insert; Trident ® Crossfire ® 10° Polyethylene Insert;System 12 Crossfire® 10° Insert; Trident® 0° Constrained Acetabular Insert; Trident® Constrained Acetabular Liner;Trident® All Poly Constrained Acetabular Insert; Crossfire® Eccentric Insert 10°; Artisan® Bone Plug;UHR® Universal Head Bipolar ComponentHowmedica Osteonics Corp., Dba Stryker Orthopaedics K243192iNSitu Lateralized Acetabular Liners, iNSitu Femoral Stems with Plasma Sprayed CPTi CoatingNextstep Arthopedix, LLC K251270Taperloc® Complete Hip StemBiomet, 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.