Medical Device Recalls
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1 result found
510(K) Number: K102392 |
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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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Globus Medical MicroFuse Putty, 2.5cc and 10cc. Product Usage: MicroFuse Bone Void Filler is ind... | 2 | 10/31/2013 | Globus Medical, Inc. |
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