Applied Osteo Systems, Inc.

FDA Regulatory Profile

Applied Osteo Systems, Inc. appears in FDA public data with 0 recalls, 15 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 21, 1995.

Summary

Total Recalls
0
510(k) Clearances
15
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K935383FEMROD AND FEMROD RECON INSERTMarch 21, 1995
K933995TRUE/FLEXTM FEMUR RODS, CAPS, SCREWS AND INSTRUMENTATIONJanuary 27, 1995
K944501TRUE/FLEX INTRAMEDULLARY ROD END-CAPNovember 28, 1994
K941048TRUE/LOK MONOLATERAL/BILATERAL FIXATOROctober 3, 1994
K943160INTERFERENCE SCREWSeptember 30, 1994
K932853PIN HOLDERS, TRANSFIXING PINS, OL WIRES, HALF PINSFebruary 22, 1994
K931578TEXAS SCOTTISH RITE EASY/LOCK FIXATORFebruary 22, 1994
K934148TRUE/FLEX CLAVICLE RODSFebruary 22, 1994
K926465FEMORAL INTRAMEDULLARY RODSAugust 25, 1993
K924657TRUE/FLEX METATARSAL RODSNovember 24, 1992
K924656TRUE/ FLEX FIBULA RODSNovember 24, 1992
K920598TRUE/FLEX HUMERUS CAPApril 28, 1992
K913949TRUE/FLEX HUMERUS, ULNA & RADIUS INTRAMED RODS SYSJanuary 17, 1992
K912710TRUE/FLEX TIBIAL RODS WITH CAPOctober 15, 1991
K902264TRUE/FLEX HUMERUS, ULNA AND RADIUS INTRAMEDULLARYJuly 12, 1990