Medical Device Manufacturer · US , Oceanside , CA

Surgitech, Inc.

2 submissions · 2 cleared · Since 2003

Total

Cleared

Denied

Surgitech, Inc. — FDA 510(k) Submissions

Surgitech, Inc. has submitted 2 FDA 510(k) premarket notifications since 2003, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Orthosis, Limb Brace, Interferential Current Therapy . Use the specialty filter in the sidebar to narrow results.

2 devices

1–2 of 2

CHRONIC PAIN SUPPRESSOR CPS-2000, MODEL CPS-2000

K033358 · LIH Interferential Current... · Neurology

Nov 2003 25d

SPARTAN ORTHOPAEDIC WRIST BRACE, MODEL SCT-1

K031576 · IQI Orthosis, Limb Brace · Physical Medicine

Jul 2003 72d

Data Source

FDA 510(k) public files . 174,402 total devices indexed.

Surgitech, Inc.

Surgitech, Inc. — FDA 510(k) Submissions

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