Clearance Summary
APS Metal Plate & Screw System received FDA 510(k) clearance under submission number K223150, sponsored by A Plus Biotechnology Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2023-08-24.
- Submission: K223150
- Applicant / Sponsor: A Plus Biotechnology Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3030
- Decision date: 2023-08-24
Classification & Regulation
This clearance is catalogued under FDA product code HRS and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.