Clearance Summary
Wiltrom Spinal Fixation System received FDA 510(k) clearance under submission number K202894, sponsored by Wiltrom Corporation Limited. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2020-10-23.
- Submission: K202894
- Applicant / Sponsor: Wiltrom Corporation Limited
- Clearance pathway: Special
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3070
- Decision date: 2020-10-23
Classification & Regulation
This clearance is catalogued under FDA product code NKB and 21 CFR 888.3070, within the Orthopedic review panel as a Class II device.