Medical Device Recalls
-
1 to 3 of 3 Results
510(K) Number: K150896 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Vitality Polyaxial Screw, 7.5mmx 50mm, REF: 07.02000.118, used with Vitality and Vital Spinal Fixati... | 2 | 01/04/2024 | Zimmer Biomet Spine Inc. |
Vitality® Spinal Fixation System. Thoracolumbosacral pedicle screw system (non-sterile). Pedicle scr... | 2 | 02/22/2019 | Zimmer Biomet Spine Inc. |
Vitality® Spinal Fixation System.Spinal Intervertebral Body, Appliance, Fixation (non-sterile). Ped... | 2 | 02/22/2019 | Zimmer Biomet Spine Inc. |
-