Medical Device Recalls
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1 result found
510(K) Number: K102156 |
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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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MAXLOCK EXTREME EXTREMITY PLATING SYSTEM WITH VARIABLE ANGLE TECHNOLOGY. Product Usage: Variabl... | 2 | 01/11/2012 | Orthohelix Surgical Designs Inc |
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