SGL
2026-06-16
Manual Instruments Designed For Use With Non-Fusion Spinous Process Tension Band Implant
FDA product code SGL · 1 cleared devices
Class 2
Orthopedic
- Regulation
- 21 CFR 888.4520
- Review panel
- OR
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 2026-06-16 – 2026-06-16
The devices are intended to manipulate tissue or implant materials for the positioning, alignment, placement, or removal of spinous process tension band implant for non-fusion use.
No matching devices.
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