Clearance Summary
PDI PARALLEL SIDED POST KIT received FDA 510(k) clearance under submission number K913019, sponsored by Precident 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 1991-10-02.
- Submission: K913019
- Applicant / Sponsor: Precident Corp.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.3810
- Decision date: 1991-10-02
Classification & Regulation
This clearance is catalogued under FDA product code ELR and 21 CFR 872.3810, within the Dental review panel as a Class I device.