General Surgical Innovations is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
General Surgical Innovations - FDA 510(k) Cleared Devices
14
Total
13
Cleared
0
Denied
General Surgical Innovations has 13 FDA 510(k) cleared general & plastic surgery devices. Based in Portola Valley, US.
Historical record: 13 cleared submissions from 1993 to 1999.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - General Surgical Innovations
14 devices
Cleared
Mar 01, 1999
FIXATION SYSTEM
General & Plastic Surgery
161d
Cleared
Jan 16, 1998
SPACEMAKER SURGICAL BALLOON DISSECTOR, SPACEMAKER II SURGICAL BALLOON...
General & Plastic Surgery
154d
Cleared
Nov 14, 1997
SPACEMAKER SURGICALBALLOON DISSECTOR/EXPANDER
General & Plastic Surgery
162d
Cleared
Apr 21, 1997
GSI CANNULA WITH INTRODUCER
Cardiovascular
90d
Cleared
Feb 19, 1997
SPACEMAKER SERIAL SURGICAL BALLOON DISSECTOR, WITH CANNULA, WITH...
General & Plastic Surgery
222d
Cleared
Sep 23, 1996
MAMMARY SIZER
General & Plastic Surgery
168d
Cleared
Aug 07, 1995
THE REUSABLE SPACEMAKER SURGICAL BALLOON DISSECTOR & CANNULA
General & Plastic Surgery
84d
Cleared
Jun 29, 1995
SPACEMAKER, II SURGICAL BALLOON DISSECTOR WITH AND WITHOUT A CANNULA
General & Plastic Surgery
84d
Cleared
Nov 01, 1994
THE SPACEMAKER AND THE SPACEMAKER II
General & Plastic Surgery
54d
Cleared
Oct 05, 1994
GSI KNOTMAKER
General & Plastic Surgery
20d
Cleared
Aug 09, 1994
GSI CANNULA REDUCER ACCESSORY
General & Plastic Surgery
14d
Cleared
Jul 07, 1994
SPECIMEN REMOVAL DEVICE
General & Plastic Surgery
114d