Valencia Pedicle Screw System 909-0010
by Altus Spine
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | NumberB41790900101 | Date28 Oct 2016 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- Valencia Pedicle Screw System
- Generic Name
- Orthopaedic instrument surgical connector
- Model / Reference
- 909-0010
- Primary DI / UDI-DI
- B41790900101
- FDA Product Code
- MNH, MNI, KWP, KWQ, NKB
- GMDN Term
- Orthopaedic instrument surgical connector
- Device Class
- Class II
- Regulation Number
- 888.3070, 888.3050, 888.3060
- GUDID distribution status
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Other devices from Altus Spine
Properties
Other properties (9)
- Sterile: No
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Serial Number: No
- Expiration Date: No