Clearance Summary
Z KAT FLUROTACTIC GUIDANCE SYSTEM MKI received FDA 510(k) clearance under submission number K984298, sponsored by Z-Kat, 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 1999-06-23.
- Submission: K984298
- Applicant / Sponsor: Z-Kat, Inc.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.4560
- Decision date: 1999-06-23
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.