Applied Osteo Systems, Inc. - FDA 510(k) Cleared Devices
15
Total
14
Cleared
0
Denied
Applied Osteo Systems, Inc. has 14 FDA 510(k) cleared orthopedic devices. Based in Moraga, US.
Historical record: 14 cleared submissions from 1990 to 1995.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
15 devices
Cleared
Mar 21, 1995
FEMROD AND FEMROD RECON INSERT
Orthopedic
498d
Cleared
Jan 27, 1995
TRUE/FLEXTM FEMUR RODS, CAPS, SCREWS AND INSTRUMENTATION
Orthopedic
528d
Cleared
Nov 28, 1994
TRUE/FLEX INTRAMEDULLARY ROD END-CAP
Orthopedic
75d
Cleared
Oct 03, 1994
TRUE/LOK MONOLATERAL/BILATERAL FIXATOR
Orthopedic
210d
Cleared
Sep 30, 1994
INTERFERENCE SCREW
Orthopedic
91d
Cleared
Feb 22, 1994
TEXAS SCOTTISH RITE EASY/LOCK FIXATOR
Orthopedic
329d
Cleared
Feb 22, 1994
PIN HOLDERS, TRANSFIXING PINS, OL WIRES, HALF PINS
Ear, Nose, Throat
257d
Cleared
Feb 22, 1994
TRUE/FLEX CLAVICLE RODS
Orthopedic
181d
Cleared
Aug 25, 1993
FEMORAL INTRAMEDULLARY RODS
Orthopedic
244d
Cleared
Nov 24, 1992
TRUE/ FLEX FIBULA RODS
Orthopedic
70d
Cleared
Nov 24, 1992
TRUE/FLEX METATARSAL RODS
Orthopedic
70d
Cleared
Apr 28, 1992
TRUE/FLEX HUMERUS CAP
Orthopedic
77d