Medical Device Recalls
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1 result found
510(K) Number: K002324 |
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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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| 5100-03-707 -- MOST Option STEM DISTRACTOR MATL: SS NONSTERILE QTY-1 Designed to facilitate intr... | 2 | 01/25/2012 |
FEI # 1000220733 Zimmer Inc. |
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