Mitek Surgical Products, Inc. - FDA 510(k) Cleared Devices
31
Total
26
Cleared
0
Denied
Mitek Surgical Products, Inc. has 26 FDA 510(k) cleared medical devices. Based in Dedham, US.
Historical record: 26 cleared submissions from 1989 to 1996. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Mitek Surgical Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Mitek Surgical Products, Inc.
31 devices
Cleared
Jan 31, 1996
MITEK THREADED ANCHOR (FASTIN)
Orthopedic
195d
Cleared
Dec 29, 1995
MITEK GII ANCHOR
Orthopedic
165d
Cleared
Oct 31, 1995
MITEK MINI ANCHOR
Gastroenterology & Urology
559d
Cleared
Oct 24, 1995
MITEK ABSORBABLE ANCHOR
Gastroenterology & Urology
571d
Cleared
Aug 02, 1995
ABSORBALBE ANCHOR
Gastroenterology & Urology
348d
Cleared
May 22, 1995
MITEK TOGGLE ANCHOR(TM)
Orthopedic
133d
Cleared
Mar 24, 1995
MITEK G III ANCHOR, MITEK LS ANCHOR
Orthopedic
169d
Cleared
Mar 06, 1995
MITEK THRADED ANCHOR (MTA)
Orthopedic
132d
Cleared
Oct 07, 1994
MITEK CANCELLOUS FIXATION SCREW, CORTICAL FIXATION SCREW, SOFT TISSUE WASHER
Orthopedic
395d
Cleared
Jul 22, 1994
MITEK GIII ANCHOR
Orthopedic
469d
Cleared
Jun 16, 1994
QUICKANCHOR II
Orthopedic
461d
Cleared
Apr 07, 1994
MITEK MODULAR DRILL BIT
General & Plastic Surgery
157d