Medical Device Recalls
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1 result found
510(K) Number: K100562 |
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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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Latitude", Tige Humerale, Humeral Stem, Medium 77 mm, Humeral Stem Right, For Cemented use only, S... | 2 | 08/29/2011 | Tornier, Inc |
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