Synvasive Technology, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Synvasive Technology, Inc. - FDA 510(k) Cleared Devices
10
Total
9
Cleared
0
Denied
Synvasive Technology, Inc. has 9 FDA 510(k) cleared orthopedic devices. Based in Rancho Cordova, US.
Historical record: 9 cleared submissions from 1994 to 2011.
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 - Synvasive Technology, Inc.
10 devices
Cleared
Mar 22, 2011
ELIBRA UNI SOFT-TISSUE FORCE SENSOR, MODEL 61-XXXX(5 MODELS, DIFFERENT SIZES
Orthopedic
538d
Cleared
Apr 04, 2007
ELIBRA DYNAMIC KNEE BALANCER
Orthopedic
83d
Cleared
Aug 26, 1997
SURGICAL BURS AND SURGICAL DRILL BITS
Orthopedic
54d
Cleared
Sep 23, 1996
KIRSCHNER WIRE (K-WIRE) AND STEINMANN PIN
Orthopedic
154d
Cleared
Aug 18, 1995
POWERGRIP(TM) COMPRESSION FIXATION DEVICE
Orthopedic
227d
Cleared
Mar 10, 1995
SPINALPLANE
Orthopedic
549d
Cleared
Apr 15, 1994
CEBOPLANE
General & Plastic Surgery
247d
Cleared
Apr 07, 1994
SYNVASIVE CERAMIC SUTTING BLOCK
Orthopedic
427d
Cleared
Mar 25, 1994
ARTHROPLANE
Orthopedic
284d
Cleared
Jan 07, 1994
HEDLEYL INTRAMEDULLARY PREPARATION BRUSH
General & Plastic Surgery
275d