Smith & Nephew Richards, Inc. - FDA 510(k) Cleared Devices
87
Total
72
Cleared
0
Denied
Smith & Nephew Richards, Inc. has 72 FDA 510(k) cleared medical devices. Based in Memphus, US.
Historical record: 72 cleared submissions from 1990 to 1997. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Smith & Nephew Richards, Inc. Filter by specialty or product code using the sidebar.
87 devices
Cleared
May 08, 1997
EMPOWER ANTERIOR DIRECT SCREWS
Orthopedic
129d
Cleared
Jan 27, 1997
GLOBAL TAPER TAPERED HIP SYSTEM, GT SPECTRON
Orthopedic
146d
Cleared
Jan 24, 1997
FINN ROD TO ROD CONNECTOR
Orthopedic
358d
Cleared
Dec 27, 1996
TRIMAX NAIL SYSTEM
Orthopedic
71d
Cleared
Dec 05, 1996
GENESIS II ZIRCONIUM FEMORAL COMPONENT/PROFIX ZIRCONIUM FEMORAL COMPONENT
Orthopedic
157d
Cleared
Nov 27, 1996
REVISION HIP SYSTEM
Orthopedic
85d
Cleared
Sep 17, 1996
REFLECTION ACETABULAR REINFORCEMENT RINGS
Orthopedic
81d
Cleared
Aug 19, 1996
ILIZAROV EXTERNAL FIXATION SYSTEM
Orthopedic
32d
Cleared
Aug 02, 1996
GENESIS II CONSTRAINED SYSTEM
Orthopedic
60d
Cleared
Apr 08, 1996
COFIED MODULAR SHOULDER SYSTEM
Orthopedic
109d
Cleared
Mar 27, 1996
REFLECTION DUAL DIMENSION SHELL
Orthopedic
76d
Cleared
Mar 11, 1996
ROGOZINSKI THORACOLUMBAR SPINAL ROD
Orthopedic
151d
Looking for a specific device from Smith & Nephew Richards, Inc.? Search by device name or K-number.
Search all Smith & Nephew... devices