Clearance Summary
KRONNER SACRAL PIN GUIDE received FDA 510(k) clearance under submission number K895172, sponsored by Kronner Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1989-09-12.
- Submission: K895172
- Applicant / Sponsor: Kronner Medical
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class I
- Regulation citation: 21 CFR 888.4540
- Decision date: 1989-09-12
Classification & Regulation
This clearance is catalogued under FDA product code LXH and 21 CFR 888.4540, within the Orthopedic review panel as a Class I device.