Clearance Summary
CAMLAB CRANIAL ORTHOSIS HELMET received FDA 510(k) clearance under submission number K081787, sponsored by Biosculptor Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2009-01-27.
- Submission: K081787
- Applicant / Sponsor: Biosculptor Corporation
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.5970
- Decision date: 2009-01-27
Classification & Regulation
This clearance is catalogued under FDA product code OAN and 21 CFR 882.5970, within the Neurology review panel as a Class II device.