Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K073708 |
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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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Accessories for the Captiva Spine SmartLOX Cervical Plate System. Products are labeled in part: ... | 2 | 05/23/2012 | Captiva Spine, Inc |
Accessories for the Captiva Spine SmartLOX Cervical Plate System. Products are labeled in part: ... | 2 | 05/23/2012 | Captiva Spine, Inc |
Instructions For Use: "***SmartLOX***Instructions for Use Cervical Plate System***STERILIZATION***T... | 2 | 05/14/2012 | Captiva Spine, Inc |
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