Clearance Summary
INTERPORE 200 POROUS HYDROXYAPATITE received FDA 510(k) clearance under submission number K852975, sponsored by Inrterpore Intl.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1985-10-31.
- Submission: K852975
- Applicant / Sponsor: Inrterpore Intl.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.5410
- Decision date: 1985-10-31
Classification & Regulation
This clearance is catalogued under FDA product code DZC and 21 CFR 872.5410, within the Dental review panel as a Class I device.