Sintea Biotech, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sintea Biotech, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Sintea Biotech, Inc. has 10 FDA 510(k) cleared orthopedic devices. Based in Miami Beach, US.
Historical record: 10 cleared submissions from 2002 to 2009.
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 - Sintea Biotech, Inc.
10 devices
Cleared
Apr 07, 2009
LAKI HAND FIXATION SYSTEM, MODEL TFX.3X.06.X
Orthopedic
204d
Cleared
Jul 18, 2008
SINTEA BIOTECH PLS MULTI-AXIAL SCREWS
Orthopedic
37d
Cleared
Jun 06, 2008
X-VOID, SPIDER
Orthopedic
304d
Cleared
Apr 18, 2007
SINTEA BIOTECH DSC/ALF SPINAL SYSTEM, DSC.XX.T5.XX, ALF.XX.T5.XX
Orthopedic
89d
Cleared
Mar 10, 2006
SINTEA BIOTECH PLS MULTI-AXIAL SCREWS, MODEL PLS.XX.T5.X
Orthopedic
11d
Cleared
Dec 17, 2004
SINTEA BIOTECH POSTERIOR LUMBAR SYSTEM WITH POLYAXIAL AND RECOVERY SCREWS,...
Orthopedic
11d
Cleared
Sep 16, 2004
SINTEA BIOTECH ANTERIOR PLATE SYSTEM, MODEL ACP.XX.T5.X
Orthopedic
55d
Cleared
Jun 24, 2003
SINTEA BIOTECH SCHANZ SCREW, MODEL TFX.SS.XX.X
Orthopedic
74d
Cleared
Dec 10, 2002
SINTEA BIOTECH POSTERIOR LUMBAR SYSTEM, MODEL PLS 00.T5.X
Orthopedic
334d
Cleared
Aug 06, 2002
SINTEA BIOTECH TRAUMAFIX SYSTEM, MODEL TFX.00.00.X
Orthopedic
42d