![](/rp/kFAqShRrnkQMbH6NYLBYoJ3lq9s.png)
The REVLOK® Fenestrated Screw System consists of monoaxial screws, uniplanar screws, polyaxial screws, dual outer diameter screws, reduction screws, rods and locking caps. Screws and rods are available in a variety of sizes to accommodate individual patient anatomy. REVLOK ® implants mate with 5.5mm diameter rods and REVLOK 6.35 implants
The REVLOK® Fenestrated Screw System consists of monoaxial screws, uniplanar screws, polyaxial screws, dual-outer-diameter screws, reduction screws, rods and locking caps. Screws and rods are available in a variety of sizes to accommodate individual patient anatomy.
Apr 2, 2018 · REVLOK ® Fenestrated Screw ... Effective date: 2018-04-02 Globus Medical, Inc. Valley Forge Business Center 2560 General Armistead Avenue Audubon, PA, 19403 United States of America De This annex is only valid in connection with the above-mentioned certificate. 3 / 4 vice family De ice Class
REVLOK Fenestrated Screw System - NordInsight
GLOBUS MEDICAL, INC. Trans-facet-screw internal spinal fixation system, sterile. The REVLOK® Fenestrated Screws have not been evaluated for safety and compatibility in the MR environment. The REVLOK® Fenestrated Screws have not been tested for heating or migration in the MR environment.
The REVLOK TM Fenestrated Screw System, when used as a posterior pedicle screw system, is intended to provide immobilization and stabilization of spinal segments in skeletally mature patients as...
AccessGUDID - DEVICE: REVLOK (00889095226010)
AccessGUDID - REVLOK (00889095226010)- 8.5mm REVLOK MIS 5.5 Screw, 70mm. Skip to Main Content; National Library of Medicine NLM Tools and Resources FDA UDI Home FDA Medical Devices Home ... Company Name: GLOBUS MEDICAL, INC. Primary DI Number: 00889095226010 Issuing Agency: GS1 Commercial Distribution End Date: Device ...
Revlok Fenestrated Screw System 510(k) FDA Premarket …
FDA premarket device registration for Revlok Fenestrated Screw System distributed by GLOBUS MEDICAL INC.
7.5mm REVLOK HA 5.5 Screw, 90mm Medical Device Identification
7.5mm REVLOK HA 5.5 Screw, 90mm GLOBUS MEDICAL, INC. FDA.report › GUDID › GLOBUS MEDICAL, INC. › 00849044070385. Trans-facet-screw internal spinal fixation system, sterile. Primary Device ID: 00849044070385: NIH Device Record Key: 16a7c765-dc23-4264-822a-87ce6f43dd19: Commercial Distribution Status:
510(k) Premarket Notification - Food and Drug Administration
Feb 3, 2025 · FORTRESS™ Radiopaque Bone Cement (FORTRESS™ and FORTRESS-Plus™), CREO® Fenestrated Screw System, REVLOK® Fenestrated Screw System Applicant Globus Medical, Inc.
Globus Medical to buy neurostim developer Nevro for $250M
1 day ago · Globus Medical’s world is about to get a little bigger, as the orthopedic devicemaker moves to acquire Nevro and its neuromodulation platforms for treating chronic pain. The all-cash deal comes ...