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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 23 of 23 Results
510(K) Number: K955848
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ORTHOFIX Catalogue Number: ref: 99-92502, PREFIX II DIAPHYSEAL COMPLETE KIT STERILE NO SCREWS, RX ... 2 11/14/2019 FEI # 3002807827
Orthofix Srl
Orthofix US XCaliber Ankle Complete Kit, Sterile, 99-91647. manufactured by Orthofix SRL, Via delle ... 2 04/28/2010 FEI # 3002807827
Orthofix Srl
Orthofix US XCaliber Meta-Diaphyseal Complete Kit, Sterile. 99-91600, manufactured by Orthofix SRL, ... 2 04/28/2010 FEI # 3002807827
Orthofix Srl
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