Clearance Summary
RESPONSE Rib and Pelvic System received FDA 510(k) clearance under submission number K233105, sponsored by OrthoPediatrics Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2024-01-20.
- Submission: K233105
- Applicant / Sponsor: OrthoPediatrics Corp.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3070
- Decision date: 2024-01-20
Classification & Regulation
This clearance is catalogued under FDA product code MDI and 21 CFR 888.3070, within the Orthopedic review panel as a Class II device.