Pathway Medical Technologies, Inc. is one of 5765 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pathway Medical Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: JETSTREAM NAVITUS L SYSTEM, JETSTREAM G3 (R) SF 1.6 SYSTEM, JETSTREAM NAVITUS SYSTEM
16
Total
16
Cleared
0
Denied
Pathway Medical Technologies, Inc. has 16 FDA 510(k) cleared cardiovascular devices. Based in Kirkland, US.
Historical record: 16 cleared submissions from 2008 to 2012.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
2 devices have linked clinical trials registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Pathway Medical Technologies, Inc.
16 devices
Cleared
CT
Feb 24, 2012
JETSTREAM NAVITUS L SYSTEM
Cardiovascular
28d
Cleared
CT
Jun 01, 2011
JETSTREAM G3 (R) SF 1.6 SYSTEM
Cardiovascular
30d
Cleared
Apr 20, 2011
JETSTREAM NAVITUS SYSTEM
Cardiovascular
47d
Cleared
Jun 11, 2010
JETSTREAM G3 SE SYSTEM, JETSTREAM G3 SF SYSTEM MODEL PV31230 (JETSTREAM G3 SE...
Cardiovascular
30d
Cleared
Jun 02, 2010
JETSTREAM G3 SYSTEM, MODEL PV31300, PV CONSOLE, MODEL PVCN100
Cardiovascular
30d
Cleared
May 19, 2010
JETSTREAM G3 L SYSTEM, PV CONSOLE, MODELS PV31400, PV31300, PVCN100
Cardiovascular
90d
Cleared
Jan 21, 2010
JETSTREAM G3 L SYSTEM MODEL PV31400 (JETSTREAM G3 L CATHETER WITH CONTROL POD)
Cardiovascular
30d
Cleared
Dec 01, 2009
JETSTREAM G3 SYSTEM
Cardiovascular
26d
Cleared
Sep 03, 2009
JETSTREAM G3 SYSTEM, MODEL PV31300 ( JETSTREAM G3 CATHETER AND CONTROL POD).,...
Cardiovascular
30d
Cleared
Jun 19, 2009
JETSTREAM G2 NXT SYSTEM, MODEL PV20300
Cardiovascular
28d
Cleared
Mar 11, 2009
JETSTREAM G2 SYSTEM, MODELS PV20300 (JETSTREAM G2 CATHETER AND CONTROL POD)
Cardiovascular
30d
Cleared
Jan 23, 2009
JETSTREAM PATHWAY PC ATHERECTOMY SYSTEM, MODEL OV10300
Cardiovascular
59d