meddevicedb.com FDA Device Reference

PASS OCT Spinal System

K160756 Class II Traditional
Decision Date
2016-04-26
Sponsor / Applicant
Medicrea International SA

Technical Specification

510(k) Submission ID K160756
Product Code NKG
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3075
Decision Date 2016-04-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PASS OCT Spinal System received FDA 510(k) clearance under submission number K160756, sponsored by Medicrea International SA. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2016-04-26.

Classification & Regulation

This clearance is catalogued under FDA product code NKG and 21 CFR 888.3075, within the Orthopedic review panel as a Class II device.