Zimmer Trabecular Metal Technology - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Zimmer Trabecular Metal Technology has 11 FDA 510(k) cleared orthopedic devices. Based in Parsippany, US.
Historical record: 11 cleared submissions from 2007 to 2014.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
11 devices
Cleared
Jul 07, 2014
VISTA-S DEVICE, ASSOCIATED INSTRUMENTATION
Orthopedic
207d
Cleared
Mar 01, 2013
TM ARDIS INTERBODY SYSTEM INSERTER
Orthopedic
100d
Cleared
Jun 29, 2012
NEXGEN LCCK TRABECULAR METAL (TM) COUPLED TIBIAL CONES PROVISIONALS TO NEXGEN...
Orthopedic
88d
Cleared
May 29, 2012
TM ARDIS INTERBODY SYSTEM TM ARDIS INTERBODY SYSTEM INSTRUMENATION
Orthopedic
180d
Cleared
Nov 18, 2011
VISTA-S DEVICE MODEL 08/06-401-XXXXX, 08/06-402-XXXXXX
Orthopedic
129d
Cleared
Jan 10, 2011
TRABECULAR METAL FUSION DEVICE MODEL 06-101-XXXXX, 06-102-XXXXX AND 08-100-XXXXX
Orthopedic
89d
Cleared
Dec 13, 2010
TRABECULAR METAL TIBIAL CONE AUGMENTS
Orthopedic
74d
Cleared
Mar 04, 2010
TRABECULAR METAL (TM) VERTEBRAL BODY REPLACEMENT (VBR) SYSTEM INSTRUMENT SET
Orthopedic
153d
Cleared
Aug 31, 2007
TRABECULAR METAL VERTEBRAL BODY REPLACEMENT (VBR), MODEL# 06-115, 06-155
Orthopedic
165d
Cleared
Jun 29, 2007
TRABECULAR METAL GLENOID- B/F COMPLETE SHOULDER SOLUTION
Orthopedic
72d
Cleared
May 30, 2007
VISTA -S DEVICE
Orthopedic
111d