meddevicedb.com FDA Device Reference

CD Horizon™ Spinal System and PASS LP™ Spinal System

K220724 Class II Special
Decision Date
2022-04-08
Sponsor / Applicant
Medicrea International

Technical Specification

510(k) Submission ID K220724
Product Code NKB
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3070
Decision Date 2022-04-08
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CD Horizon™ Spinal System and PASS LP™ Spinal System received FDA 510(k) clearance under submission number K220724, sponsored by Medicrea International. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2022-04-08.

Classification & Regulation

This clearance is catalogued under FDA product code NKB and 21 CFR 888.3070, within the Orthopedic review panel as a Class II device.