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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K093293
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Vanguard 360 Revision System Posterior Augment With Bolt - Product Usage: intended for use in knee a... 2 12/23/2020 Biomet, Inc.
Vanguard 360 Revision Knee System 63x 10mm Universal Tibial Block Augment, Model Number 185221 ... 2 09/25/2018 Zimmer Biomet, Inc.
Vanguard 360 Revision Knee System 75x 5mm Universal Tibial Block Augment, Model Number 185224 I... 2 09/25/2018 Zimmer Biomet, Inc.
Vanguard 360 Revision Knee System Knee prostheses 2 10/03/2016 Zimmer Biomet, Inc.
Vanguard 360 Femoral Boss Reamer, Label: REF 32-488474 VANGUARD 360 1NSTRUMENT FEMORAL BOSS REAM... 2 08/15/2014 Biomet, Inc.
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