Clearance Summary
ACE FISCHER EXTERNAL FIXATION DEVICE received FDA 510(k) clearance under submission number K801594, sponsored by Ace Orthopedic Manufacturing Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1980-09-09.
- Submission: K801594
- Applicant / Sponsor: Ace Orthopedic Manufacturing Co.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class I
- Regulation citation: 21 CFR 888.4540
- Decision date: 1980-09-09
Classification & Regulation
This clearance is catalogued under FDA product code HXK and 21 CFR 888.4540, within the Orthopedic review panel as a Class I device.