Clearance Summary
KENSEY NASH FIBRILLAR COLLAGEN DENTAL MEMBRANE received FDA 510(k) clearance under submission number K090919, sponsored by Kensey Nash Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2009-10-02.
- Submission: K090919
- Applicant / Sponsor: Kensey Nash Corp.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3930
- Decision date: 2009-10-02
Classification & Regulation
This clearance is catalogued under FDA product code NPL and 21 CFR 872.3930, within the Dental review panel as a Class II device.