ELEVATE™ Spinal System 8657002
by Medtronic Sofamor Danek, Inc. 2 variants
ELEVATE™ Spinal System 8657002 is a Class II device made by Medtronic Sofamor Danek, Inc., cleared under FDA 510(k) K142559 on 9 Jun 2015 and listed in FDA GUDID since 27 Jul 2025 (UDI-DI 00763000880262), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00763000880262 | Date27 Jul 2025 | StatusListed |
| United States | FDA 510(k)SESE | NumberK142559 | Date9 Jun 2015 | StatusActive |
Official records
- AccessGUDID record 00763000880262
- FDA 510(k) database K142559
Across registries
- FDA 510(k) K142559 decided 9 Jun 2015 Active
- FDA GUDID UDI-DI 00763000880262 listed 27 Jul 2025 Listed
Timeline
- Cleared FDA 510(k) K142559
- Listed FDA GUDID 00763000880262
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- ELEVATE™ Spinal System
- Generic name
- Orthopaedic inorganic implant inserter/extractor, reusable
- Model / reference
- 8657002
- Primary DI / UDI-DI
- 00763000880262
- 510(k) Number
- FDA product code
- MAX
- GMDN term
- Orthopaedic inorganic implant inserter/extractor, reusable
- Device class
- Class II
- Regulation number
- 888.3080
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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