Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K963951 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| BioHorizons 0.050 Hex Driver, Regular, REF 300-350, BioHorizons Implant Systems, Inc., Birmingham, A... | 3 | 04/13/2007 | BioHorizons Implant Systems Inc |
| BioHorizons 0.050 Hex Driver, Long, REF 300-351, BioHorizons Implant Systems, Inc., Birmingham, AL ... | 3 | 04/13/2007 | BioHorizons Implant Systems Inc |
| BioHorizons 0.035 Hex Driver, REF 300-377, BioHorizons Implant Systems, Inc., Birmingham, AL 35243,... | 3 | 04/13/2007 | BioHorizons Implant Systems Inc |
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