FDA 510(k)

PRECISION HIP SYSTEM PROXIMAL FEMORAL SPACER #6259

K-Number: K860442 · 1986-05-06

Decision Date1986-05-06

Product CodeLPH

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

PRECISION HIP SYSTEM PROXIMAL FEMORAL SPACER #6259 is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1986-05-06 under 510(k) number K860442. 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 PRECISION HIP SYSTEM PROXIMAL FEMORAL SPACER #6259?

PRECISION HIP SYSTEM PROXIMAL FEMORAL SPACER #6259 is a medical device that received FDA 510(k) clearance on 1986-05-06. The listed applicant is Howmedica Corp.. The 510(k) number is K860442.

When did PRECISION HIP SYSTEM PROXIMAL FEMORAL SPACER #6259 receive FDA 510(k) clearance?

PRECISION HIP SYSTEM PROXIMAL FEMORAL SPACER #6259 received FDA 510(k) clearance on 1986-05-06, under 510(k) number K860442.

Who is the listed applicant for PRECISION HIP SYSTEM PROXIMAL FEMORAL SPACER #6259?

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

What is the FDA product code for PRECISION HIP SYSTEM PROXIMAL FEMORAL SPACER #6259?

The FDA product code for PRECISION HIP SYSTEM PROXIMAL FEMORAL SPACER #6259 is LPH.

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Other records listing Howmedica Corp. as applicant

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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.