Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K221403 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Cortera Spinal Fixation System, REF: 150100-85050. Spinal fixation screws labeled as 8.5 mm diameter... | 2 | 01/29/2024 |
FEI # 3005031160 XTANT Medical Holdings, Inc |
| Cortera Spinal Fixation System Screw, Poly, Solid, 6.5mm x 45mm, REF: 150100-65045 | 2 | 10/17/2024 |
FEI # 3005031160 XTANT Medical Holdings, Inc |
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