Clearance Summary
Baide received FDA 510(k) clearance under submission number K150009, sponsored by Jiangsu Baide Medical Intrument 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 2015-02-25.
- Submission: K150009
- Applicant / Sponsor: Jiangsu Baide Medical Intrument Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3030
- Decision date: 2015-02-25
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.