Vital™ 804M9000
Vital™ 804M9000 is a Class II device made by Biomet Spine LLC, listed in FDA GUDID since 29 Oct 2019 (UDI-DI 00887868314490), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00887868314490 | Date29 Oct 2019 | StatusListed |
Official records
- AccessGUDID record 00887868314490
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Vital™
- Generic name
- Bone-screw internal spinal fixation system, non-sterile
- Model / Ref / Catalog
- 804M9000
- Primary DI / UDI-DI
- 00887868314490
- FDA product code
- NKB
- GMDN term
- Bone-screw internal spinal fixation system, non-sterile
- Device class
- Class II
- Regulation number
- 888.3070
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices
Other devices filed under FDA product code NKB (Thoracolumbosacral pedicle screw system).
- CD Horizon™ ModuLeX™ Spinal System G25031500 by MEDTRONIC SOFAMOR DANEK, INC.
- Erisma™-LP 18415512 by Clariance, Inc.
- Tsrh Spinal System by MEDTRONIC SOFAMOR DANEK, INC.
- Synthes Pangea Monoaxial System by Synthes Spine Co.Lp
- FORTEZZA Spinal Stabilization System by Osso Surgical
- Erisma®-LP 18505100 by Clariance, Inc.
- Iliad® Pedicle Screw System and Zenius® Pedicle Screw System by Medyssey USA, Inc.
- Europa Pedicle Screw System by MIRUS LLC
- PERLA ® TL MIS MPF-MH PX 00-S by Spineart
- Altus Spine Pedicle Screw System by Altus Partners