Medos International SARL - FDA 510(k) Cleared Devices
Recent clearances: CROSSNAV Navigation Enabled Instruments for Disc Preparation and Interbody, SYMPHONY Navigation Ready Instruments, TriALTIS™ Spine System
97
Total
97
Cleared
0
Denied
FDA 510(k) Regulatory Record - Medos International SARL Neurology ✕
13 devices
Cleared
Feb 10, 2023
TELIGEN System Peripheral Motor Nerve Stimulation Indications
Neurology
88d
Cleared
Jul 14, 2022
CEREPAK Uniform, Uniform XL, Uniform 3D, Heliform Soft, Heliform XtraSoft,...
Neurology
190d
Cleared
Apr 12, 2022
PROWLER SELECT LP ES Microcatheter
Neurology
111d
Cleared
Aug 25, 2021
PROWLER SELECT PLUS
Neurology
156d
Cleared
May 28, 2021
MICRUSFRAME, DELTAFILL, DELTAXSFT, GALAXY G3, GALAXY G3 XSFT, and GALAXY G3...
Neurology
25d
Cleared
Feb 27, 2020
CEREBASE DA Guide Sheath, 95cm, CEREBASE DA Guide Sheath, 90cm, CEREBASE DA...
Neurology
149d
Cleared
Apr 05, 2018
SENTIO MMG Gen 2
Neurology
142d
Cleared
Mar 22, 2018
SENTIO MMG Pedicle Access Needles
Neurology
174d
Cleared
Jan 22, 2016
DirectLink ICP Module, DirectLink ICP Extension Cable, Patient Monitor...
Neurology
127d
Cleared
Oct 27, 2015
Codman Certas Plus Programmable Valve
Neurology
85d
Cleared
Feb 19, 2015
Codman Certas Plus Programmable Valve
Neurology
113d
Cleared
Feb 16, 2012
CODMAN CERTAS PROGRAMMABLE VALVE SYSTEM
Neurology
78d
Cleared
Oct 17, 2011
CODMAN CERTAS PROGRAMMABLE VALVE SYSTEM, CODMAN CERTAS THERAPY MANAGEMENT SYSTEM
Neurology
82d