Clearance Summary
ORTHOPEDIC LOWER EXTREMITY SUSPENSION received FDA 510(k) clearance under submission number K801436, sponsored by Orthopedic Systems, Inc.. 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 1980-06-26.
- Submission: K801436
- Applicant / Sponsor: Orthopedic Systems, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.3910
- Decision date: 1980-06-26
Classification & Regulation
This clearance is catalogued under FDA product code FYH and 21 CFR 878.3910, within the General, Plastic Surgery review panel as a Class I device.