Clearance Summary
CUTTER, P606 BONE received FDA 510(k) clearance under submission number K770302, sponsored by Dentronix, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1977-03-09.
- Submission: K770302
- Applicant / Sponsor: Dentronix, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4800
- Decision date: 1977-03-09
Classification & Regulation
This clearance is catalogued under FDA product code FZT and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.