FDA 510(k)

PERFECTA RS LATERALIZED HIP STEM, BRIDGE HIP SYSTEM

K-Number: K991123 · 1999-06-01

Decision Date1999-06-01

Product CodeLPH

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

PERFECTA RS LATERALIZED HIP STEM, BRIDGE HIP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 1999-06-01 under 510(k) number K991123. 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 PERFECTA RS LATERALIZED HIP STEM, BRIDGE HIP SYSTEM?

PERFECTA RS LATERALIZED HIP STEM, BRIDGE HIP SYSTEM is a medical device that received FDA 510(k) clearance on 1999-06-01. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K991123.

When did PERFECTA RS LATERALIZED HIP STEM, BRIDGE HIP SYSTEM receive FDA 510(k) clearance?

PERFECTA RS LATERALIZED HIP STEM, BRIDGE HIP SYSTEM received FDA 510(k) clearance on 1999-06-01, under 510(k) number K991123.

Who is the listed applicant for PERFECTA RS LATERALIZED HIP STEM, BRIDGE HIP SYSTEM?

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

What is the FDA product code for PERFECTA RS LATERALIZED HIP STEM, BRIDGE HIP SYSTEM?

The FDA product code for PERFECTA RS LATERALIZED HIP STEM, BRIDGE HIP SYSTEM 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

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