Clearance Summary
Medtronic Legend Pneumatic; MR7 Pneumatic; Triton Pneumatic Drill System incorporating various Pneumatic Handpieces; Attachments; Surgical Dissecting Tools; and System Accessories received FDA 510(k) clearance under submission number K163182, sponsored by Medtronic Powered Surgical Solutions. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2017-03-23.
- Submission: K163182
- Applicant / Sponsor: Medtronic Powered Surgical Solutions
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.4370
- Decision date: 2017-03-23
Classification & Regulation
This clearance is catalogued under FDA product code HBB and 21 CFR 882.4370, within the Neurology review panel as a Class II device.