Cousin Biotech Sas - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Cousin Biotech Sas has 6 FDA 510(k) cleared medical devices. Based in Wervicq-Sud, FR.
Historical record: 6 cleared submissions from 2008 to 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Cousin Biotech Sas Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Cousin Biotech Sas
6 devices
Cleared
Jan 09, 2019
Cortical Fixation Systems
Orthopedic
259d
Cleared
Aug 29, 2018
ResCUBE™ Ligament Fixation System
Orthopedic
55d
Cleared
Apr 10, 2018
NAJA™ Ligament Correction System
Orthopedic
263d
Cleared
Sep 04, 2014
PREMIUM
General & Plastic Surgery
258d
Cleared
Jun 25, 2010
BIOMESH CA.B.S. 'AIR COMPOSITE, MODELS: CABST1R05T, CABSAIRC7, CABSAIRC09
General & Plastic Surgery
259d
Cleared
Jun 26, 2008
CABS'AIR
General & Plastic Surgery
251d