Discectomy Set 102-59-01
Discectomy Set 102-59-01 (100-1298) is a Class I device made by Spineology Inc., listed in FDA GUDID since 16 Apr 2025 (UDI-DI M7401001298), registry data as of 23 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 | NumberM7401001298 | Date16 Apr 2025 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Discectomy Set
- Generic name
- Intermittent powered traction system
- Model / Ref / Catalog
- 102-59-01, 100-1298
- Primary DI / UDI-DI
- M7401001298
- FDA product code
- LXH
- GMDN term
- Intermittent powered traction system
- Device class
- Class I
- Regulation number
- 888.4540
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- MRI safety
- MR Unsafe
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