Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K073303 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Norian Drillable Inject | 2 | 02/15/2018 | Synthes USA |
Norian Drillable Inject 5 CC-Sterile; catalog # 07.704.005S Intended for bony voids or defects of t... | 2 | 06/09/2016 | Synthes (USA) Products LLC |
Norian Drillable Inject 10 CC-Sterile; catalog # 07.704.010S Intended for bony voids or defects of ... | 2 | 06/09/2016 | Synthes (USA) Products LLC |
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