Smith & Nephew Dyonics, Inc. - FDA 510(k) Cleared Devices
22
Total
19
Cleared
0
Denied
FDA 510(k) Regulatory Record - Smith & Nephew Dyonics, Inc. Orthopedic ✕
16 devices
Cleared
Feb 08, 1996
LIMITED REUSE ARTHROSCOPIC BLADES
Orthopedic
55d
Cleared
Dec 18, 1995
ECTRA II LIGAMENT RELEASE SYSTEM
Orthopedic
73d
Cleared
Sep 15, 1995
DYONICS DISPOSABLE ARTHROSCOPIC BLADES
Orthopedic
38d
Cleared
Aug 09, 1995
ECTRA LIGAMENT RELEASE SYSTEM
Orthopedic
21d
Cleared
Jan 24, 1995
DYONICS FIXATION SCREWS
Orthopedic
92d
Cleared
Feb 14, 1994
DYONICS DISPOSABLE ARTHROSCOPIC SURGERY BLADES MODIFICATION
Orthopedic
165d
Cleared
Jun 04, 1992
SMITH & NEPHEW DYONICS TMJ ARTHROSCOPY INFLOW SET
Orthopedic
212d
Cleared
Mar 06, 1992
SUCTION CONTROL FOOTSWITCH WITH SPEED CONTROL
Orthopedic
220d
Cleared
Feb 18, 1992
SMALL JOINT SYSTEM
Orthopedic
126d
Cleared
Sep 18, 1991
PALMER ARCH SUPPRESSOR
Orthopedic
54d
Cleared
Aug 26, 1991
INTELIJET TM FLUID MANAGEMENT SYSTEM
Orthopedic
84d
Cleared
Dec 05, 1990
ARTHROSCOPIC SURGICAL BLADE
Orthopedic
79d
Cleared
Oct 12, 1990
MODIFIED ENDOSCOPIC CARPAL TUNNEL RELEASE SYSTEM
Orthopedic
66d
Cleared
Jun 25, 1990
POSTEROMEDIAL GUIDE
Orthopedic
68d
Cleared
Jun 20, 1990
CANNULATED INTERFERENCE SCREW SYSTEM
Orthopedic
75d
Cleared
Apr 18, 1990
ARTHROSCOPIC ELECTROSURGICAL PROBE
Orthopedic
19d