Medical Device Recalls
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1 result found
510(K) Number: K030827 |
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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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Universal Optical Tracker Fixation, not sterile, Manufactured by Orthosoft, Montreal, Canada, REF 11... | 2 | 09/20/2008 | Zimmer Inc. |
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