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Innerspace, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K113088HUMMINGBIRD SUBDURAL H900DS (DRAINAGE AND ICP), HUMMINGBIRD SUBDURAL- H800S (ICP ONLY)May 2, 2012
K083378SYNERGYSeptember 29, 2009
K072379MPS OXIPORT AND MPS OXIPORT PLUSApril 29, 2008
K041838MPS (OR MPS-T)March 1, 2005
K013705ACT III VENTRICULAR CATHETERSeptember 9, 2002
K013005ACT 11 MP VENTRICULAR CATHETERMarch 8, 2002
K010422ACT II ICP MONITORING SYSTEM AND VENTRICULAR CATHETERJune 28, 2001
K003905ACTI-ICP MONITORING SYSTEMJune 15, 2001