Future Medical Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Future Medical Systems, Inc. - FDA 510(k) Cleared Devices
12
Total
11
Cleared
0
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
Cleared
May 05, 2003
ADHOC CLAW
Orthopedic
157d
Cleared
Jun 25, 2002
TITANIUM CANNULATED INTERFERENCE SCREW
Orthopedic
88d
Cleared
Jan 18, 2002
PLLA CANNULATED INTERFERENCE SCREW
Orthopedic
72d
Cleared
Sep 11, 2000
FMS SOLO
Orthopedic
68d
Cleared
May 08, 1998
ENDO FMS UROLOGY
Gastroenterology & Urology
66d
Cleared
Feb 05, 1996
FMS ARTHOPROBE
Orthopedic
66d
Cleared
Nov 09, 1995
FMS DUO
Orthopedic
45d
Cleared
Oct 23, 1995
ARTHROPLAST & ARTHRO-CUTTER
Orthopedic
45d
Cleared
Jul 14, 1995
REF. 4102CV INTERMEDIARY TUBING, REF. 4509CV STERILE ZONE KIT
Orthopedic
85d
Cleared
May 12, 1995
FMS HIGH FLOW ARTHRO-SHEATH
Ophthalmic
30d
Cleared
May 09, 1995
FMS ARTHRO-CUTTER
Ophthalmic
27d
Cleared
Mar 22, 1995
FMS ARTHROSCOPY CANNULA
Orthopedic
104d