Disco-O-Tech Medical Technologies, Ltd. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Disco-O-Tech Medical Technologies, Ltd. has 9 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 9 cleared submissions from 1999 to 2003. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Disco-O-Tech Medical Technologies, Ltd. Filter by specialty or product code using the sidebar.
9 devices
Cleared
Sep 12, 2003
MODIFICATION TO FIXION INTRAMEDULLARY NAILING SYSTEM (FIXION IM)
Orthopedic
21d
Cleared
Aug 06, 2003
FIXION DYNAMIC HIP SCREW SYSTEM (FIXION DHS)
Orthopedic
93d
Cleared
Nov 14, 2002
FIXION INTERLOCKING PROXIMAL FEMUR INTRAMEDULLARY NAILING SYSTEM (FIXION PF...
Orthopedic
30d
Cleared
May 23, 2002
FIXION INTRAMEDULLARY NAILING SYSTEM (FIXION IM NAILING SYSTEM)
Orthopedic
27d
Cleared
Oct 04, 2001
MODIFICATION TO FIXION INTERLOCKING PROXIMAL FEMORAL INTRAMEDULLARY NAILING...
Orthopedic
30d
Cleared
Dec 28, 2000
FIXION INTRAMEDULLARY NAILING SYSTEM (FIXION IM NAIL)
Orthopedic
76d
Cleared
Dec 27, 2000
MODIFICATION OF FIXION INTRAMEDULLARY NAILING SYSTEM (FIXION IM NAIL)
Orthopedic
75d
Cleared
Dec 05, 2000
FIXION INTERLOCKING NAIL (FIXION IL NAIL)
Orthopedic
90d
Cleared
Jun 02, 1999
FIXION INTRAMEDULLARY NAILING SYSTEM
Orthopedic
90d