Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K240749 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| PILLAR SA Ti, STERILE, 37mm (W) x 28mm (D) x 18mm (H), 20-degrees, REF: 82-3713SP | 2 | 09/11/2025 |
FEI # 2183449 Orthofix U.S. LLC |
| Orthofix Pillar SA Ti Spacer System Intervertebral Body Fusion Spinal Device, sterile, implant grade... | 2 | 03/21/2025 |
FEI # 2183449 Orthofix U.S. LLC |
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