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FDA 510(k) Applications Submitted by MITEK WORLDWIDE
FDA 510(k) Number
Submission Date
Device Name
Applicant
K032167
07/16/2003
BIO-INTRAFIX TIBIAL SCREW AND SHEATH
MITEK WORLDWIDE
K032717
09/02/2003
BIOCRYL RAPIDE INTERFERENCE SCREW
MITEK WORLDWIDE
K021953
06/13/2002
MITEK PDS/PGA STAPLE
MITEK WORLDWIDE
K023388
10/09/2002
MITEK RAPIDLOC-PDS MENISCAL REPAIR SYSTEM
MITEK WORLDWIDE
K030995
03/31/2003
MINILOK QUICKANCHOR PLUS
MITEK WORLDWIDE
K031519
05/15/2003
CUFFLOK ANCHOR
MITEK WORLDWIDE
K021883
06/07/2002
BIOFASTIN RC THREADED SUTURE ANCHOR
MITEK WORLDWIDE
K024115
12/13/2002
MICROFIX QUICKANCHOR PLUS
MITEK WORLDWIDE
K031406
05/05/2003
EXOJET TISSUE MANAGEMENT SYSTEM
MITEK WORLDWIDE
K032078
07/07/2003
MITEK MICRO QUICKANCHOR
MITEK WORLDWIDE
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