Surgical Dynamics, Inc. - FDA 510(k) Cleared Devices
12
Total
9
Cleared
0
Denied
Surgical Dynamics, Inc. has 9 FDA 510(k) cleared medical devices. Based in San Leandro, US.
Historical record: 9 cleared submissions from 1989 to 1996. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Surgical Dynamics, Inc. Filter by specialty or product code using the sidebar.
12 devices
Cleared
Apr 02, 1996
SURGICAL DYNAMICS 30K WORKING CHANNEL SCOPE
Orthopedic
91d
Cleared
Oct 30, 1995
NUCLEOTOME L KIT
General & Plastic Surgery
497d
Cleared
Oct 23, 1995
SURGICAL DYNAMICS 30K WORKING CHANNEL SCOPE & INSTRUMENT SET
Orthopedic
47d
Cleared
May 09, 1995
SUGICAL DYNAMICS ENDOSCOPY IRRIGATION PUMP, CATALOG #3-4000
General & Plastic Surgery
92d
Cleared
Mar 29, 1994
NUCLEOTOME E KIT
Orthopedic
391d
Cleared
Jun 07, 1993
SURGICAL DYNAMICS DISCOGRAPHY SYSTEM
General Hospital
406d
Cleared
Feb 09, 1993
NUCLEOTOME 3.5 MM AUTOMATED PERCUTANEOUS LUMBAR
Orthopedic
208d
Cleared
Dec 19, 1991
NUCLEOTOME TISSUE ASPIRATOR/CUTTER
Orthopedic
156d
Cleared
Dec 19, 1991
NUCLEOTOME(R) II (VERSION2) TISSUE ASPIRA/CUTTER
Orthopedic
86d
Cleared
Oct 30, 1990
SURGICAL DYNAMICS NUCLEOTOME II TISSUE ASPIR/CUTER
Orthopedic
127d
Cleared
Aug 04, 1989
SURGICAL DYNAMICS DISCOGRAPHY SYSTEM
General & Plastic Surgery
21d
Cleared
May 01, 1989
HEMATOME SYSTEM
General & Plastic Surgery
146d