FDA 510(k), K162770, Relign System

510(K) Number: K162770
Device Name: Relign System
Manufacturer: Relign Corporation
Device Classification Name: Electrosurgical, Cutting & Coagulation & Accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 10/03/2016
Decision Date: 01/04/2017
Regulation Medical Specialty: General & Plastic Surgery

503 pages (3,597 of 4,100 original pages are fully redacted)