Clearance Summary
PEGASUS DENTAL ALLOY received FDA 510(k) clearance under submission number K962302, sponsored by Sterngold/Implamed. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1996-07-18.
- Submission: K962302
- Applicant / Sponsor: Sterngold/Implamed
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3060
- Decision date: 1996-07-18
Classification & Regulation
This clearance is catalogued under FDA product code EJT and 21 CFR 872.3060, within the Dental review panel as a Class II device.