Clearance Summary
TEMPLATE received FDA 510(k) clearance under submission number K873470, sponsored by Cox-Uphuff Intl.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1987-09-08.
- Submission: K873470
- Applicant / Sponsor: Cox-Uphuff Intl.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4800
- Decision date: 1987-09-08
Classification & Regulation
This clearance is catalogued under FDA product code FTY and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.