Medical Device Manufacturer · US , Dedham , MA

Mitek Surgical Products, Inc. - FDA 510(k) Cleared Devices

31 submissions · 26 cleared · Since 1989

Total

Cleared

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) Regulatory Record - Mitek Surgical Products, Inc.

31 devices

1-12 of 31

Cleared Jan 31, 1996

MITEK THREADED ANCHOR (FASTIN)

Gastroenterology & Urology · 559d

Cleared Oct 24, 1995

MITEK ABSORBABLE ANCHOR

K941599 · MNV

Gastroenterology & Urology · 571d

Cleared Aug 02, 1995

ABSORBALBE ANCHOR

K944051 · MNV

Gastroenterology & Urology · 348d

Cleared May 22, 1995

MITEK TOGGLE ANCHOR(TM)

K950070 · JDR

Orthopedic · 133d

Cleared Mar 24, 1995

MITEK G III ANCHOR, MITEK LS ANCHOR

K944936 · JDR

Orthopedic · 169d

Cleared Mar 06, 1995

MITEK THRADED ANCHOR (MTA)

K945203 · JDR

Orthopedic · 132d

Cleared Oct 07, 1994

MITEK CANCELLOUS FIXATION SCREW, CORTICAL FIXATION SCREW, SOFT TISSUE WASHER

MITEK MODULAR DRILL BIT

K935225 · GFG

General & Plastic Surgery · 157d

Mitek Surgical Products, Inc. - FDA 510(k) Cleared Devices

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