Clearance Summary
ZIMMER ONE-PIECE IMPLANT, 3.7 MM, ANGLED received FDA 510(k) clearance under submission number K061717, sponsored by Zimmer Dental, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2006-09-08.
- Submission: K061717
- Applicant / Sponsor: Zimmer Dental, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3640
- Decision date: 2006-09-08
Classification & Regulation
This clearance is catalogued under FDA product code DZE and 21 CFR 872.3640, within the Dental review panel as a Class II device.