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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 12 Results
510(K) Number: K171768
 
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TRIDENTII HEMI CLUSTER44B- Indicated for use in primary and revision patients at high risk of hip d... 2 04/25/2024 Howmedica Osteonics Corp.
TRIDENTII HEMI CLUSTER48D-indicated for use in primary and revision patients at high risk of hip dis... 2 04/25/2024 Howmedica Osteonics Corp.
TRIDENTII HEMI CLUSTER50D- Indicated for use in primary and revision patients at high risk of hip di... 2 04/25/2024 Howmedica Osteonics Corp.
TRIDENTII HEMI CLUSTER52E-Indicated for use in primary and revision patients at high risk of hip dis... 2 04/25/2024 Howmedica Osteonics Corp.
TRIDENTII HEMI CLUSTER54E- Indicated for use in primary and revision patients at high risk of hip d... 2 04/25/2024 Howmedica Osteonics Corp.
TRIDENTII PSL CLUSTER64H- Indicated for use in primary and revision patients at high risk of hip dis... 2 04/25/2024 Howmedica Osteonics Corp.
TRIDENTII HEMI CLUSTER66H- Indicated for use in primary and revision patients at high risk of hip d... 2 04/25/2024 Howmedica Osteonics Corp.
TRIDENTII PSL CLUSTER48D- Indicated for use in primary and revision patients at high risk of hip di... 2 04/25/2024 Howmedica Osteonics Corp.
TRIDENTII PSL CLUSTER50D- Indicated for use in primary and revision patients at high risk of hip dis... 2 04/25/2024 Howmedica Osteonics Corp.
TRIDENTII PSL CLUSTER52E- Indicated for use in primary and revision patients at high risk of hip dis... 2 04/25/2024 Howmedica Osteonics Corp.
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