FDA 510(k)

TRI-LOCK HIP STEM

K-Number: K001982 · 2000-07-26

Decision Date2000-07-26

Product CodeLPH

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

TRI-LOCK HIP STEM is the device name listed in this FDA 510(k) record. The listed applicant is DePuy Orthopaedics, Inc.. It received FDA 510(k) clearance on 2000-07-26 under 510(k) number K001982. 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 TRI-LOCK HIP STEM?

TRI-LOCK HIP STEM is a medical device that received FDA 510(k) clearance on 2000-07-26. The listed applicant is DePuy Orthopaedics, Inc.. The 510(k) number is K001982.

When did TRI-LOCK HIP STEM receive FDA 510(k) clearance?

TRI-LOCK HIP STEM received FDA 510(k) clearance on 2000-07-26, under 510(k) number K001982.

Who is the listed applicant for TRI-LOCK HIP STEM?

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

What is the FDA product code for TRI-LOCK HIP STEM?

The FDA product code for TRI-LOCK HIP STEM is LPH.

Other records listing DePuy Orthopaedics, Inc. as applicant

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.

K262130ATTUNE Revision Knee System K252887DePuy ATTUNE™ Knee System K231503CUPTIMIZE™ Advanced K213839DePuy Corail AMT Hip Prosthesis K210167DELTA XTEND Reverse Shoulder System K203167DePuy Corail AMT Hip Prosthesis

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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

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