Zimmer Biomet Spine Inc.
5 FDA 510(k) clearances · Recalling firm
◉ Watch Zimmer Biomet Spine Inc.
| Record | Firm | Date |
|---|---|---|
| Vitality Polyaxial Screw, 7.5mmx 50mm, REF: 07.02000.118, used with Vitality and Vital Spi recall (Z-0639-2024) | Zimmer Biomet Spine Inc. | 2024-01-04 |
| Vitality Spinal Fixation System. Thoracolumbosacral pedicle screw system (non-sterile). Pe recall (Z-0866-2019) | Zimmer Biomet Spine Inc. | 2019-02-22 |
| Vitality Spinal Fixation System. Spinal Interlaminal, Appliance, Fixation, (non-sterile). recall (Z-0867-2019) | Zimmer Biomet Spine Inc. | 2019-02-22 |
| Vitality Spinal Fixation System.Spinal Intervertebral Body, Appliance, Fixation (non-steri recall (Z-0868-2019) | Zimmer Biomet Spine Inc. | 2019-02-22 |
| Vitality Spinal Fixation System, Vitality T27 Final Drivers and Vitality Torque Limiting H recall (Z-2318-2017) | Zimmer Biomet Spine Inc. | 2017-05-15 |
Track Zimmer Biomet Spine Inc. automatically
Every clearance here is in the API, with alerts when new ones post.