Clearance Summary
Phantom Fukushima Neurological Holding Systems, Phantom Mastability Neurological Holding Systems received FDA 510(k) clearance under submission number K161318, sponsored by Tedan Surgical Innovations, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2017-03-20.
- Submission: K161318
- Applicant / Sponsor: Tedan Surgical Innovations, LLC
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.4800
- Decision date: 2017-03-20
Classification & Regulation
This clearance is catalogued under FDA product code GZT and 21 CFR 882.4800, within the Neurology review panel as a Class II device.