Clearance Summary
OSSEOSPEED 4.0S-6MM, MODEL 24619 received FDA 510(k) clearance under submission number K063779, sponsored by Astra Tech, 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 2007-04-27.
- Submission: K063779
- Applicant / Sponsor: Astra Tech, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3640
- Decision date: 2007-04-27
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.