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FDA 510(k)

CEMENTED CALCAR HIP SYSTEM

K-Number: K013490 · 2002-01-17

ApplicantEncore Orthopedics, Inc.
Decision Date2002-01-17
Product CodeLPH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CEMENTED CALCAR HIP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Encore Orthopedics, Inc.. It received FDA 510(k) clearance on 2002-01-17 under 510(k) number K013490. 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 CEMENTED CALCAR HIP SYSTEM?

CEMENTED CALCAR HIP SYSTEM is a medical device that received FDA 510(k) clearance on 2002-01-17. The listed applicant is Encore Orthopedics, Inc.. The 510(k) number is K013490.

When did CEMENTED CALCAR HIP SYSTEM receive FDA 510(k) clearance?

CEMENTED CALCAR HIP SYSTEM received FDA 510(k) clearance on 2002-01-17, under 510(k) number K013490.

Who is the listed applicant for CEMENTED CALCAR HIP SYSTEM?

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

What is the FDA product code for CEMENTED CALCAR HIP SYSTEM?

The FDA product code for CEMENTED CALCAR HIP SYSTEM is LPH.

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Other records listing Encore Orthopedics, 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.

K0329053DKNEE POROUS COATED FEMORAL COMPONENTK0201143D KNEEK020741UNICONDYLAR KNEEK020236MODIFICATION TO PASS SPINAL SYSTEMK020170KEYSTONE HIP SYSTEM CALCAR REPLACEMENT BODY AND BUILD UPK013442PASS SPINAL SYSTEM

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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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