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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 13 of 13 Results
510(K) Number: K830196
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VERSA-FXII SC TUBE PLT 90DX16H, 95DX16H, 95DX18H, 95DX20H, 95DX22H 2 06/15/2017 Zimmer Biomet, Inc.
VERSA-FX II STD TUBE 130DX16H, 130DX18H, 130DX20H, 135DX16H, 135DX18H, 135DX20H, 140DX16H, 140DX... 2 06/15/2017 Zimmer Biomet, Inc.
4.5 BROAD SCP PLT 26-H STER 2 06/15/2017 Zimmer Biomet, Inc.
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