Clearance Summary
ALLOTROPAT/HEYLTEX CORP. BONE GRAFTING DENSE HYDRO received FDA 510(k) clearance under submission number K850012, sponsored by Heyltex 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 1985-04-22.
- Submission: K850012
- Applicant / Sponsor: Heyltex Corp.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3930
- Decision date: 1985-04-22
Classification & Regulation
This clearance is catalogued under FDA product code LYC and 21 CFR 872.3930, within the Dental review panel as a Class II device.