Instratek, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Instratek, Inc. has 10 FDA 510(k) cleared orthopedic devices. Based in Houston, US.
Historical record: 10 cleared submissions from 1992 to 2014.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
10 devices
Cleared
Feb 06, 2014
STAPIX SUPERELASTIC IMPLANT BONE STAPLES
Orthopedic
83d
Cleared
Jul 25, 2013
JONES-FX FRACTURE SYSTEM
Orthopedic
52d
Cleared
May 17, 2012
MINI CANNULATED HEADED AND HEADLESS SCREW SET
Orthopedic
90d
Cleared
Aug 31, 2011
CMC CABLE FIX
Orthopedic
140d
Cleared
Aug 14, 2009
MICHELANGELO BUNION SYSTEM - MABS, MODEL: MA6000
Orthopedic
59d
Cleared
Dec 08, 2008
HAV-LOK BUNION CORRECTION SYSTEM
Orthopedic
111d
Cleared
Mar 14, 2008
SUB-TALAR LOK, MODEL 7-11 MM
Orthopedic
39d
Cleared
Dec 12, 1994
ENDOSCOPIC MORTONS NEUROMA INSTRUMENTS
Orthopedic
332d
Cleared
Apr 27, 1993
ENDOTRAK SYSTEM
Orthopedic
202d
Cleared
Aug 18, 1992
ENDOSCOPIC CARPAL TUNNEL INSTRUMENTS
Orthopedic
90d