Clearance Summary
SPINAL MICROKNIFE received FDA 510(k) clearance under submission number K882525, sponsored by Karlin Technology, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1988-09-22.
- Submission: K882525
- Applicant / Sponsor: Karlin Technology, Inc.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class I
- Regulation citation: 21 CFR 888.4540
- Decision date: 1988-09-22
Classification & Regulation
This clearance is catalogued under FDA product code HTS and 21 CFR 888.4540, within the Orthopedic review panel as a Class I device.