Clearance Summary
TRIGEN INTERTAN 10S Nail System received FDA 510(k) clearance under submission number K241804, sponsored by Smith & Nephew, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2024-08-22.
- Submission: K241804
- Applicant / Sponsor: Smith & Nephew, Inc.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3030
- Decision date: 2024-08-22
Classification & Regulation
This clearance is catalogued under FDA product code JDS and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.