Clearance Summary
CEDAR(TM) RETRACTOR RING received FDA 510(k) clearance under submission number K873691, sponsored by Cedar Surgical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1987-09-28.
- Submission: K873691
- Applicant / Sponsor: Cedar Surgical, Inc.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.4800
- Decision date: 1987-09-28
Classification & Regulation
This clearance is catalogued under FDA product code GZT and 21 CFR 882.4800, within the Neurology review panel as a Class II device.