Smith & Nephew, Inc., Orthopaedic Div. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Smith & Nephew, Inc., Orthopaedic Div. - FDA 510(k) Cleared Devices
10
Total
8
Cleared
0
Denied
Smith & Nephew, Inc., Orthopaedic Div. has 8 FDA 510(k) cleared orthopedic devices. Based in Memphis, US.
Historical record: 8 cleared submissions from 1996 to 1999.
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 - Smith & Nephew, Inc., Orthopaedic Div.
10 devices
Cleared
Jun 03, 1999
OPERA CUPFLANGED ACETABULAR COMPONENTS
Orthopedic
31d
Cleared
Aug 14, 1997
TITANIUM SPINAL ROD SYSTEM
Orthopedic
175d
Cleared
Jul 16, 1997
ZIRCONIA PROZYR CERAMIC 12/14 GLOBAL TAPER (GT) FEMORAL HEADS
Orthopedic
91d
Cleared
May 09, 1997
TAYLOR SPATIAL FRAME EXTERNAL FIXATION SYSTEM
Orthopedic
67d
Cleared
Apr 16, 1997
HEIDELBERG EXTERNAL FIXATOR
Orthopedic
44d
Cleared
Apr 03, 1997
COMPASS UNIVERSAL HINGE
Orthopedic
35d
Cleared
Feb 28, 1997
HA GLOBAL TAPER (GT) TAPERED HIP STEM
Orthopedic
30d
Cleared
Feb 28, 1997
GLOBAL TAPER SPECTRON HIP STEMS
Orthopedic
29d
Cleared
Jan 02, 1997
PROFIX PLUS TIBIAL INSERT, PROFIX PS PLUS TIBIAL INSERT, PROFIX P/S TIBIAL...
Orthopedic
136d
Cleared
Oct 02, 1996
ULTIUM SPINAL PLATING SYSTEM
Orthopedic
77d