ELEVATE™ Spinal System 8881032
by Medtronic Sofamor Danek, Inc.
ELEVATE™ Spinal System 8881032 is a Class II device made by Medtronic Sofamor Danek, Inc., cleared under FDA 510(k) K172199 on 19 Sep 2017 (1 earlier submission) and listed in FDA GUDID since 6 Nov 2015 (UDI-DI 00643169430877), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK172199 | Date19 Sep 2017 | StatusActive |
| United States | GUDID listing | Number00643169430877 | Date6 Nov 2015 | StatusListed |
Official records
- AccessGUDID record 00643169430877
- FDA 510(k) database K172199
- FDA 510(k) database K142559
Across registries
- FDA 510(k) K172199 decided 19 Sep 2017 Active
- FDA GUDID UDI-DI 00643169430877 listed 6 Nov 2015 Listed
Timeline
- Cleared FDA 510(k) K142559
- Listed FDA GUDID 00643169430877
- Cleared FDA 510(k) K172199
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- ELEVATE™ Spinal System
- Generic name
- Polymeric spinal interbody fusion cage
- Model / reference
- 8881032
- Primary DI / UDI-DI
- 00643169430877
- FDA product code
- MAX
- GMDN term
- Polymeric spinal interbody fusion cage
- Device class
- Class II
- Regulation number
- 888.3080
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Conditional
- Size
- Length — 32.0 MillimeterWidth — 10.0 MillimeterHeight — 10.0 Millimeter
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