Peak Surgical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Peak Surgical, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Peak Surgical, Inc. has 7 FDA 510(k) cleared medical devices. Based in Palo Alto, US.
Historical record: 7 cleared submissions from 2008 to 2011. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Peak Surgical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Peak Surgical, Inc.
7 devices
Cleared
May 27, 2011
PEAK SUCTION COAGULATOR
General & Plastic Surgery
151d
Cleared
Dec 17, 2010
PEAK PLASMABLADE PLUS TISSUE DISSECTION DEVICE
General & Plastic Surgery
88d
Cleared
Dec 16, 2010
PEAK PULSAR II GENERATOR MODEL PS100-102
General & Plastic Surgery
150d
Cleared
Apr 13, 2010
PEAK PLASMABLADE 3.OS TISSUE DISSECTION DEVICE
General & Plastic Surgery
134d
Cleared
Jun 05, 2009
PEAK PLASMABLADE TNA TONSIL AND ADENOID TISSUE DISSECTION DEVICE
General & Plastic Surgery
199d
Cleared
Dec 03, 2008
PULSAR GENERATOR, PEAK PLASMABLADE
General & Plastic Surgery
71d
Cleared
Jul 22, 2008
PULSAR GENERATOR, MODEL PS100-100, AND PEAK PLASMABLADE TISSUE DISSECTION...
General & Plastic Surgery
266d