Turnkey Intergration USA, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Turnkey Intergration USA, Inc. - FDA 510(k) Cleared Devices
26
Total
23
Cleared
0
Denied
Turnkey Intergration USA, Inc. has 23 FDA 510(k) cleared orthopedic devices. Based in Indianapolis, US.
Historical record: 23 cleared submissions from 1990 to 1999.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Turnkey Intergration USA, Inc.
26 devices
Cleared
Jun 29, 1999
OMNI-FIX, HUMERAL NAIL
Orthopedic
68d
Cleared
Apr 30, 1999
B2C, ESPACE REVISION CUP SYSTEM
Orthopedic
70d
Cleared
Apr 01, 1999
OMNI-FIX, NAIL SYSTEM
Orthopedic
59d
Cleared
Aug 29, 1997
LINK CEMENT PLUG
Orthopedic
64d
Cleared
Apr 21, 1997
ARTOS, DIPLOS SYSTEM
Orthopedic
87d
Cleared
Mar 13, 1997
LINK CERCLAGE WIRE SYSTEM
Orthopedic
63d
Cleared
Nov 06, 1995
LUBINUS SP II HIP SYSTEM
Orthopedic
95d
Cleared
Jul 05, 1995
LINK ENDO MODEL REVISION CUP
Orthopedic
323d
Cleared
May 25, 1995
LINK SADDLE PROTHESIS
Orthopedic
78d
Cleared
Apr 14, 1995
SYSTEM 22 VALVE
Anesthesiology
72d
Cleared
Feb 06, 1995
UNIVERSAL WRIST
Orthopedic
381d
Cleared
Jan 26, 1995
LINK SADDLE PROTHESIS
General & Plastic Surgery
203d