Clearance Summary
AMSET(TM) BONE SCREW received FDA 510(k) clearance under submission number K911768, sponsored by Advanced Med/Surg, 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 1991-10-04.
- Submission: K911768
- Applicant / Sponsor: Advanced Med/Surg, Inc.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3040
- Decision date: 1991-10-04
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.