Scholten Surgical Instruments, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Scholten Surgical Instruments, Inc. has 8 FDA 510(k) cleared medical devices. Based in Redwood City, US.
Historical record: 8 cleared submissions from 1985 to 2007. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Scholten Surgical Instruments, Inc. Filter by specialty or product code using the sidebar.
8 devices
Cleared
Oct 03, 2007
NOVATOME, MODEL: SU101-50
Cardiovascular
69d
Cleared
Mar 01, 1990
SCHOLTEN FRAME
General & Plastic Surgery
31d
Cleared
Aug 01, 1986
SYS, ANGIOGRAPHIC, SINGLE-OR BI-PLANE RADIOGRAPHIC
Radiology
427d
Cleared
Sep 15, 1985
TEMPORARY PACEMAKER GROUND WIRE
Cardiovascular
123d
Cleared
Jul 02, 1985
FORCEPS, BIOPSY(NON RIGID)
General & Plastic Surgery
48d
Cleared
Jul 02, 1985
TABLE ACCESSORIES, OPERATING ROOM
General & Plastic Surgery
32d
Cleared
Jun 27, 1985
RETRACTOR, SURGICAL
General & Plastic Surgery
27d
Cleared
Jun 14, 1985
STAND, OPERATING ROOM
General Hospital
14d