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FDA 510(k) Applications Submitted by EDWARD F KENT
FDA 510(k) Number
Submission Date
Device Name
Applicant
K970119
01/14/1997
MITEK ABSORBABLE POLYDIOXANONE (PDS) H FIX
MITEK PRODUCTS
K970360
01/31/1997
MITEK SUTURE RETROGRADER
MITEK PRODUCTS
K961094
03/14/1996
MITEK THREADED ANCHOR (MODIFICATION)
MITEK PRODUCTS
K982420
06/15/1998
MITEK MICRO ANCHOR
MITEK PRODUCTS
K962511
06/27/1996
MITEK MICRO ANCHOR
MITEK PRODUCTS
K962793
07/17/1996
MITEK MICRO ANCHOR
MITEK PRODUCTS
K953560
07/20/1995
MITEK THREADED ANCHOR (FASTIN)
MITEK SURGICAL PRODUCTS, INC.
K973009
08/13/1997
MITEK NON ABSORBABLE POLYPROPYLENE H FIX
MITEK PRODUCTS
K963783
09/20/1996
MITEK ELECTROSURGICAL SYSTEM FOR ARTHROSCOPIC USE
ETHICON, INC.
K964013
10/07/1996
MITEK ABSORBABLE TOGGLE ANCHOR
MITEK PRODUCTS
K974022
10/14/1997
VAPR
MITEK PRODUCTS
K983818
10/29/1998
MITEK FASTIN RC ANCHOR
MITEK PRODUCTS
K974291
11/14/1997
MITEK BTB ABSORBABLE (PLA) CROSS PIN
MITEK PRODUCTS
K974345
11/19/1997
MITEK KNOTLESS ANCHOR
MITEK PRODUCTS
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