Theken Surgical,Llc - FDA 510(k) Cleared Devices
6
Total
4
Cleared
0
Denied
Theken Surgical,Llc has 4 FDA 510(k) cleared medical devices. Based in Barberton, US.
Historical record: 4 cleared submissions from 1998 to 2005. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Theken Surgical,Llc Filter by specialty or product code using the sidebar.
6 devices
Cleared
May 17, 2005
THEKEN REVEAL VBR SYSTEM
Orthopedic
126d
Cleared
Feb 20, 2004
THEKEN CPOD/LPOD VERTEBRAL BODY REPLACEMENT SYSTEM
Orthopedic
232d
Cleared
Oct 29, 2001
THEKEN LARGE CEMENT RESTRICTOR
Orthopedic
89d
Cleared
Oct 17, 2001
THEKEN SMALL CEMENT RESTRICTOR
Orthopedic
90d
Cleared
May 16, 2001
TETHER ACFS
Orthopedic
89d
Cleared
Dec 30, 1998
BODYFORM THORACO-LUMBAR FIXATION SYSTEM
Orthopedic
76d