Spiracur, Inc. - FDA 510(k) Cleared Devices
9
Total
8
Cleared
1
Denied
Spiracur, Inc. has 8 FDA 510(k) cleared medical devices. Based in Philadelphia, US.
Historical record: 8 cleared submissions from 2009 to 2015. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Spiracur, Inc. Filter by specialty or product code using the sidebar.
9 devices
Cleared
Nov 19, 2015
SNaP Wound Care System
General & Plastic Surgery
148d
Cleared
Nov 25, 2014
SNaP Wound Care System
General & Plastic Surgery
102d
Cleared
Mar 12, 2014
SNAP WOUND CARE SYSTEM
General & Plastic Surgery
250d
Cleared
Feb 25, 2014
CISNAP CLOSED INCISION SYSTEM
General & Plastic Surgery
137d
Cleared
Dec 01, 2011
SNAP WOUND CARE SYSTEM
General & Plastic Surgery
50d
Cleared
Aug 29, 2011
SNAP WOUND CARE SYSTEM
General & Plastic Surgery
14d
Cleared
Jul 28, 2011
SNAP (R) WOUND CARE SYSTEM
General & Plastic Surgery
71d
Cleared
Jul 21, 2011
CI-SNAP WOUND CARE SYSTEM
General & Plastic Surgery
101d
Not Cleared
Aug 07, 2009
SNAP WOUND CARE DEVICE
General & Plastic Surgery
277d