meddevicedb.com FDA Device Reference

EXPEDIUM Spine System/Synapse System

K142460 Class II Special
Decision Date
2014-10-01
Sponsor / Applicant
Johnson and Johnson

Technical Specification

510(k) Submission ID K142460
Product Code KWP
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3050
Decision Date 2014-10-01
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EXPEDIUM Spine System/Synapse System received FDA 510(k) clearance under submission number K142460, sponsored by Johnson and Johnson. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2014-10-01.

Classification & Regulation

This clearance is catalogued under FDA product code KWP and 21 CFR 888.3050, within the Orthopedic review panel as a Class II device.