Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K171907 |
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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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Vitality® Spinal Fixation System. Spinal Interlaminal, Appliance, Fixation, (non-sterile). Pedicle s... | 2 | 02/22/2019 | Zimmer Biomet Spine Inc. |
Vitality® Spinal Fixation System. Thoracolumbosacral pedicle screw system (non-sterile). Pedicle scr... | 2 | 02/22/2019 | Zimmer Biomet Spine Inc. |
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