Metagen, LLC - FDA 510(k) Cleared Devices
Recent clearances: METAGEN ACTIVELOCK WIRE CERCLAGE SYSTEM, SEGMENTAL DEFECT REPLACEMENT SYSTEM, ACTIVELOCK MODULAR FEMORAL HIP SYSTEM
5
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Metagen, LLC Orthopedic ✕
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