Clearance Summary
PEC IMPLANT received FDA 510(k) clearance under submission number K913768, sponsored by Applied Biomaterial Technologies. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 1992-02-03.
- Submission: K913768
- Applicant / Sponsor: Applied Biomaterial Technologies
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class II
- Regulation citation: 21 CFR 874.3620
- Decision date: 1992-02-03
Classification & Regulation
This clearance is catalogued under FDA product code MIC and 21 CFR 874.3620, within the Ear, Nose, Throat review panel as a Class II device.