Innerspace, Inc. is one of 19620 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Innerspace, Inc. - FDA 510(k) Cleared Devices
Recent clearances: HUMMINGBIRD SUBDURAL H900DS (DRAINAGE AND ICP), HUMMINGBIRD SUBDURAL- H800S (ICP ONLY), SYNERGY, MPS OXIPORT AND MPS OXIPORT PLUS
8
Total
8
Cleared
0
Denied
Innerspace, Inc. has 8 FDA 510(k) cleared medical devices. Based in Santa Ana, US.
Historical record: 8 cleared submissions from 2001 to 2012. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Innerspace, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Innerspace, Inc.
8 devices
Cleared
May 02, 2012
HUMMINGBIRD SUBDURAL H900DS (DRAINAGE AND ICP), HUMMINGBIRD SUBDURAL- H800S...
Neurology
196d
Cleared
Sep 29, 2009
SYNERGY
Neurology
319d
Cleared
Apr 29, 2008
MPS OXIPORT AND MPS OXIPORT PLUS
Neurology
249d
Cleared
Mar 01, 2005
MPS (OR MPS-T)
Neurology
237d
Cleared
Sep 09, 2002
ACT III VENTRICULAR CATHETER
Neurology
305d
Cleared
Mar 08, 2002
ACT 11 MP VENTRICULAR CATHETER
Neurology
183d
Cleared
Jun 28, 2001
ACT II ICP MONITORING SYSTEM AND VENTRICULAR CATHETER
Neurology
136d
Cleared
Jun 15, 2001
ACTI-ICP MONITORING SYSTEM
Neurology
178d