Clearance Summary
ATRISORB BIOABSORBABLE GUIDED TISSUE REGNERATION(GTR) received FDA 510(k) clearance under submission number K955838, sponsored by Atrix Laboratories, 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 1996-03-21.
- Submission: K955838
- Applicant / Sponsor: Atrix Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3930
- Decision date: 1996-03-21
Classification & Regulation
This clearance is catalogued under FDA product code NPK and 21 CFR 872.3930, within the Dental review panel as a Class II device.