Clearance Summary
CRANIAL MOLDING ORTHOSIS received FDA 510(k) clearance under submission number K010273, sponsored by Orthotic Solutions, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2001-04-25.
- Submission: K010273
- Applicant / Sponsor: Orthotic Solutions, Inc.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.5970
- Decision date: 2001-04-25
Classification & Regulation
This clearance is catalogued under FDA product code MVA and 21 CFR 882.5970, within the Neurology review panel as a Class II device.