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Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)

FDA product code JDL · Class 3 · Orthopedic

575
Registered devices
3,884
Adverse events
4
Recalls
45
510(k) clearances

Devices with this code

CONSERVE® — Microport Orthopedics Inc.Consensus Hip System — Shalby Advanced Technologies, Inc.Consensus® Hip System — CONSENSUS ORTHOPEDICS, INC.Arcos Modular Revision Hip System — Biomet Orthopedics, LLCHEALEY HIP SYSTEM — Biomet Orthopedics, LLCDuracon — Howmedica Osteonics Corp.CONSERVE® — Microport Orthopedics Inc.Fitmore® Hip Stem — Zimmer GmbHOmnifit — Howmedica Osteonics Corp.Compress Device — Biomet Orthopedics, LLCHEALEY HIP SYSTEM — Biomet Orthopedics, LLCConsensus® Hip System — CONSENSUS ORTHOPEDICS, INC.Arcos Modular Revision Hip System — Biomet Orthopedics, LLCOmnifit — Howmedica Osteonics Corp.Taperloc — Biomet Orthopedics, LLCHEALEY HIP SYSTEM — Biomet Orthopedics, LLCTaperloc Complete Hip System — Biomet Orthopedics, LLCFitmore® Hip Stem — Zimmer GmbHCONSERVE® — Microport Orthopedics Inc.TRANSCEND® — Microport Orthopedics Inc.Omnifit — Howmedica Osteonics Corp.Fitmore® Hip Stem — Zimmer GmbHConsensus® Hip System — CONSENSUS ORTHOPEDICS, INC.TAPERLOC MICROPLASTY INSTRUMENTATION — Biomet Uk Ltd

Recent recalls

DateFirmReason
2010-06-07Wright Medical Technology IncThe inner and outer product packaging was missing the following information: shelf life, translations, manufacturing date, CE marking and also listed the incor
2009-05-14Wright Medical Technology IncIncorrect packaging, swapped sizes
2009-05-14Wright Medical Technology IncIncorrect packaging, swapped sizes
2004-01-09Stryker Howmedica OsteonicsThis device is not approved for sale in the US.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.