Medical Device Recalls
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1 result found
510(K) Number: K022325 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Normed TX 8 Driver, Non-Cannulated (used with the Ascension Total Foot System); Catalog #503004268; ... | 2 | 06/26/2009 | Ascension Orthopedics, Inc |
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