Medical Device Recalls
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1 result found
510(K) Number: K123623 |
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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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| Illico Ti Cannulated Polyaxial Screw 7.5mm X 40mm. The Illico MIS Posterior Fixation System is inten... | 2 | 08/27/2013 |
FEI # 2027467 Alphatec Spine, Inc. |
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