Clearance Summary
SKULL MOUNTED STEREOTACTIC SURGICAL DEVICE received FDA 510(k) clearance under submission number K851659, sponsored by Medco Products, Co., 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 1985-07-01.
- Submission: K851659
- Applicant / Sponsor: Medco Products, Co., Inc.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.4560
- Decision date: 1985-07-01
Classification & Regulation
This clearance is catalogued under FDA product code HAW and 21 CFR 882.4560, within the Neurology review panel as a Class II device.