Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K051942 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Malibu Polyaxial Screw, 7.5 x 35mm Part Number 12-7535 Malibu Spinal System when used as a Pedicl... | 2 | 09/03/2009 | SeaSpine, Inc |
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