Spirus Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Spirus Medical, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Spirus Medical, Inc. has 5 FDA 510(k) cleared medical devices. Based in Ayer, US.
Historical record: 5 cleared submissions from 2005 to 2008. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Spirus Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Spirus Medical, Inc.
5 devices
Cleared
May 06, 2008
SPIRUS MEDICAL ENDO-EASE ENDOSCOPIC OVERTUBE
Gastroenterology & Urology
119d
Cleared
Apr 03, 2008
SPIRUS MEDICAL SURGICAL INSTRUMENT
General Hospital
86d
Cleared
Oct 13, 2006
MODIFICATION TO ENDO-EASE
Gastroenterology & Urology
24d
Cleared
Aug 04, 2006
ENDO-EASE ENDOSCOPIC OVERTUBE
Gastroenterology & Urology
186d
Cleared
Sep 14, 2005
ENDO-EASE ENDOSCOPIC OVERTUBE
Gastroenterology & Urology
43d