Metagen, LLC - FDA 510(k) Cleared Devices
5
Total
4
Cleared
0
Denied
Metagen, LLC has 4 FDA 510(k) cleared medical devices. Based in Menomonie, US.
Historical record: 4 cleared submissions from 1997 to 1998. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Metagen, LLC Filter by specialty or product code using the sidebar.
5 devices
Cleared
Dec 30, 1998
METAGEN ACTIVELOCK WIRE CERCLAGE SYSTEM
Orthopedic
51d
Cleared
May 18, 1998
SEGMENTAL DEFECT REPLACEMENT SYSTEM
Orthopedic
90d
Cleared
Apr 03, 1998
ACTIVELOCK MODULAR FEMORAL HIP SYSTEM
Orthopedic
88d
Cleared
Mar 21, 1997
METAGEN ALL POLY ACETABULAR CUP SYSTEM
Orthopedic
165d
Cleared
Feb 12, 1997
METAGEN HIGH TIBIAL OSTEOTOMY SYSTEM
Orthopedic
149d