Medical Device Recalls
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1 result found
510(K) Number: K173524 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| ANAX 5.5 Poly-Reduction Screw 6.0X50MM, REF: SFNA6050R, part of ANAX 5.5 SPINAL SYSTEM | 2 | 07/20/2020 |
FEI # 3003200961 U&I CORP. |
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