Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K113079 |
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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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Hemostatic Bone Putty, for use as a water-soluble implant material and for use in the control of bl... | 2 | 02/11/2015 | Synthes, Inc. |
Synthes(R) Hemostatic Bone Putty, Part numbers 08.901.001.97S, 08.901.001.98S, 08.901.001.99S, 08.90... | 1 | 08/16/2012 | Synthes USA HQ, Inc. |
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