Clearance Summary
Syntec Non-Sterile Steinmann Pins System received FDA 510(k) clearance under submission number K200933, sponsored by Syntec Scientific Corporation. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2020-05-05.
- Submission: K200933
- Applicant / Sponsor: Syntec Scientific Corporation
- Clearance pathway: Special
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3040
- Decision date: 2020-05-05
Classification & Regulation
This clearance is catalogued under FDA product code JDW and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.