Mitek Worldwide is one of 24554 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mitek Worldwide - FDA 510(k) Cleared Devices
Recent clearances: BIOCRYL RAPIDE INTERFERENCE SCREW, BIO-INTRAFIX TIBIAL SCREW AND SHEATH, MITEK MICRO QUICKANCHOR
10
Total
10
Cleared
0
Denied
Mitek Worldwide has 10 FDA 510(k) cleared orthopedic devices. Based in Norwood, US.
Historical record: 10 cleared submissions from 2002 to 2004.
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 - Mitek Worldwide
10 devices
Cleared
Mar 31, 2004
BIOCRYL RAPIDE INTERFERENCE SCREW
Orthopedic
211d
Cleared
Oct 15, 2003
BIO-INTRAFIX TIBIAL SCREW AND SHEATH
Orthopedic
91d
Cleared
Aug 25, 2003
MITEK MICRO QUICKANCHOR
Orthopedic
49d
Cleared
Jun 26, 2003
MINILOK QUICKANCHOR PLUS
Orthopedic
87d
Cleared
Jun 06, 2003
CUFFLOK ANCHOR
Orthopedic
22d
Cleared
May 30, 2003
EXOJET TISSUE MANAGEMENT SYSTEM
Orthopedic
25d
Cleared
Mar 13, 2003
MICROFIX QUICKANCHOR PLUS
Orthopedic
90d
Cleared
Dec 27, 2002
MITEK RAPIDLOC-PDS MENISCAL REPAIR SYSTEM
Orthopedic
79d
Cleared
Dec 20, 2002
MITEK PDS/PGA STAPLE
Orthopedic
190d
Cleared
Jul 01, 2002
BIOFASTIN RC THREADED SUTURE ANCHOR
Orthopedic
24d