Acclarent, Inc. - FDA 510(k) Cleared Devices
45
Total
44
Cleared
1
Denied
FDA 510(k) cleared devices by Acclarent, Inc. General & Plastic Surgery ✕
8 devices
Cleared
Oct 07, 2011
RELIEVA STRATUS PRO MICROFLOW SPACER (FRONTAL)
General & Plastic Surgery
210d
Cleared
Mar 03, 2010
MODIFICATION TO RELIEVA STRATUS MICROFLOW SPACER
General & Plastic Surgery
104d
Cleared
Jan 29, 2009
RELIEVA STRATUS MICROFLOW SPACER
General & Plastic Surgery
57d
Cleared
Mar 19, 2008
SINUS SPACER
General & Plastic Surgery
161d
Cleared
Mar 11, 2008
RELIEVA AND RELIEVA ACELLA SINUS BALLOON CATHETER
General & Plastic Surgery
134d
Cleared
Sep 28, 2007
RELIEVA LUMA SINUS ILLUMINATION SYSTEM, MODEL SIS-100A
General & Plastic Surgery
85d
Cleared
Sep 15, 2006
ETHMOID SINUS SPACER
General & Plastic Surgery
23d
Cleared
May 05, 2006
RELIENT NAVIGATION DEVICE
General & Plastic Surgery
25d