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FDA 510(k)

EUROPEAN STYLE TAPER,PRESS-FIT HIP STEM

K-Number: K062775 · 2007-01-16

ApplicantOrtho Development Corp.
Decision Date2007-01-16
Product CodeLPH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

EUROPEAN STYLE TAPER,PRESS-FIT HIP STEM is the device name listed in this FDA 510(k) record. The listed applicant is Ortho Development Corp.. It received FDA 510(k) clearance on 2007-01-16 under 510(k) number K062775. 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 EUROPEAN STYLE TAPER,PRESS-FIT HIP STEM?

EUROPEAN STYLE TAPER,PRESS-FIT HIP STEM is a medical device that received FDA 510(k) clearance on 2007-01-16. The listed applicant is Ortho Development Corp.. The 510(k) number is K062775.

When did EUROPEAN STYLE TAPER,PRESS-FIT HIP STEM receive FDA 510(k) clearance?

EUROPEAN STYLE TAPER,PRESS-FIT HIP STEM received FDA 510(k) clearance on 2007-01-16, under 510(k) number K062775.

Who is the listed applicant for EUROPEAN STYLE TAPER,PRESS-FIT HIP STEM?

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

What is the FDA product code for EUROPEAN STYLE TAPER,PRESS-FIT HIP STEM?

The FDA product code for EUROPEAN STYLE TAPER,PRESS-FIT HIP STEM is LPH.

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Other records listing Ortho Development Corp. 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.

K253161Balanced Knee System TriMax Porous Femoral ComponentsK251052Trivicta® Hip StemK242984BKS Revision SystemK242833Legend® Acetabular ShellK233758Trivicta™ Hip StemK131022OVATION 10/12 HIP STEM

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Related Devices (Code: LPH)

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.

K261453G7® Acetabular SystemZimmer BiometK253630Mpact 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 OrthopaedicsK243192iNSitu Lateralized Acetabular Liners, iNSitu Femoral Stems with Plasma Sprayed CPTi CoatingNextstep Arthopedix, LLCK251270Taperloc® 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.

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