Clearance Summary
FILLOCK REAMER received FDA 510(k) clearance under submission number K901097, sponsored by Ivoclar North America, 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 1990-04-25.
- Submission: K901097
- Applicant / Sponsor: Ivoclar North America, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.4130
- Decision date: 1990-04-25
Classification & Regulation
This clearance is catalogued under FDA product code DZA and 21 CFR 872.4130, within the Dental review panel as a Class I device.