Mitek Products - FDA 510(k) Cleared Devices
30
Total
30
Cleared
0
Denied
Mitek Products has 30 FDA 510(k) cleared orthopedic devices. Based in Westwood, US.
Historical record: 30 cleared submissions from 1996 to 2002.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
30 devices
Cleared
Mar 14, 2002
MITEK BIOCRYL INTERFERENCE SCREWS
Orthopedic
136d
Cleared
Feb 06, 2002
RIDIDFIX 2.7MM BTB CROSS PIN KIT
Orthopedic
84d
Cleared
May 11, 2001
BIOKNOTLESS ANCHOR
General & Plastic Surgery
260d
Cleared
May 09, 2001
RIGIDFIX SOFT TISSUE ACL CROSSPIN SYSTEM
Orthopedic
68d
Cleared
Feb 15, 2001
MITEK 2GII MENISCAL REPAIR SYSTEM
Orthopedic
192d
Cleared
Oct 27, 2000
MITEK CUFFTACK
Orthopedic
24d
Cleared
Aug 31, 2000
VAPR TC ELECTRODE FOR USE WITH VAPR II ELECTROSURGICAL SYSTEM
Orthopedic
24d
Cleared
Aug 31, 2000
VARPR 3.5MM 90 SUCTION ELECTRODE FOR USE WITH VAPR SYSTEM
General & Plastic Surgery
23d
Cleared
Apr 19, 2000
VAPR 2.3MM WEDGE ELECTRODE FOR USE WITH VAPR SYSTEM
General & Plastic Surgery
27d
Cleared
Dec 29, 1999
RESOLVE QUICKANCHOR
Dental
69d
Cleared
Dec 16, 1999
TALON ANCHOR SNAP-PAK
Dental
73d
Cleared
Dec 02, 1999
TALON ANCHOR SNAP-PAK
Orthopedic
64d