Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K172456 |
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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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REF 8420.15.010, Bone Screw/Vite - Ti6AI4V, Self Tapping/Autofilettante, Dia=6.5mm, h=20mm, STERILE ... | 2 | 10/21/2021 | Limacorporate S.p.A |
REF 8420.15.020, Bone Screw/Vite - Ti6AI4V, Self Tapping/Autofilettante, Dia=6.5mm, h=25mm, STERILE ... | 2 | 10/21/2021 | Limacorporate S.p.A |
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