meddevicedb.com FDA Device Reference

Statera-C™ Spinal System

K233332 Class II Traditional
Decision Date
2023-11-27
Sponsor / Applicant
K&J Consulting Corp.

Technical Specification

510(k) Submission ID K233332
Product Code NKG
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3075
Decision Date 2023-11-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Statera-C™ Spinal System received FDA 510(k) clearance under submission number K233332, sponsored by K&J Consulting Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2023-11-27.

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.