Medical Device Manufacturer · US , New York City , NY

Future Medical Systems, Inc. - FDA 510(k) Cleared Devices

12 submissions · 11 cleared · Since 1995

Total

Cleared

Denied

Future Medical Systems, Inc. has 11 FDA 510(k) cleared orthopedic devices. Based in New York City, US.

Historical record: 11 cleared submissions from 1995 to 2003.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Future Medical Systems, Inc.

12 devices

1-12 of 12

TITANIUM CANNULATED INTERFERENCE SCREW

K021030 · HWC

Orthopedic · 88d

Cleared Jan 18, 2002

PLLA CANNULATED INTERFERENCE SCREW

Gastroenterology & Urology · 66d

ARTHROPLAST & ARTHRO-CUTTER

K954217 · HRX

Orthopedic · 45d

Cleared Jul 14, 1995

REF. 4102CV INTERMEDIARY TUBING, REF. 4509CV STERILE ZONE KIT

K951843 · HRX

Orthopedic · 85d

Cleared May 12, 1995

FMS HIGH FLOW ARTHRO-SHEATH

FMS ARTHROSCOPY CANNULA

K945973 · HRX

Orthopedic · 104d

Future Medical Systems, Inc. - FDA 510(k) Cleared Devices

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