Medical Device Recalls
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1 result found
510(K) Number: K112757 |
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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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| STREAMLINE CT CERVICO-THORACIC SYSTEM; SET SCREW REF 26-SETSCREW NON-STERILE, SINGLE USE, RX ONLY ... | 2 | 09/03/2014 |
FEI # 1000115331 PIONEER SURGICAL TECHNOLOGY, INC. |
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