Clearance Summary
Asnis III Cannulated Screw System, Asnis PRO Cannulated Screw System received FDA 510(k) clearance under submission number K220319, sponsored by Stryker GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2022-06-10.
- Submission: K220319
- Applicant / Sponsor: Stryker GmbH
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3040
- Decision date: 2022-06-10
Classification & Regulation
This clearance is catalogued under FDA product code HWC and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.