Clearance Summary
PERMA FIBER,MODEL 441; PERMA MESH, MODEL 440 received FDA 510(k) clearance under submission number K082180, sponsored by Angelus Industria DE Productos Odontologicos. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2008-12-17.
- Submission: K082180
- Applicant / Sponsor: Angelus Industria DE Productos Odontologicos
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3760
- Decision date: 2008-12-17
Classification & Regulation
This clearance is catalogued under FDA product code EBI and 21 CFR 872.3760, within the Dental review panel as a Class II device.