Clearance Summary
NEURO SECTOR FIXATION DEVICE received FDA 510(k) clearance under submission number K833522, sponsored by Advanced Technology Laboratories, 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 1984-05-25.
- Submission: K833522
- Applicant / Sponsor: Advanced Technology Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.1240
- Decision date: 1984-05-25
Classification & Regulation
This clearance is catalogued under FDA product code GXW and 21 CFR 882.1240, within the Neurology review panel as a Class II device.