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MODIFICATION TO NEUROSENSOR CEREBRAL BLOOD FLOW AND INTRACRANIAL PRESSURE MONITORING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071505
510(k) Type
Traditional
Applicant
INTEGRA LIFESCIENCES CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/6/2007
Days to Decision
66 days
Submission Type
Summary

MODIFICATION TO NEUROSENSOR CEREBRAL BLOOD FLOW AND INTRACRANIAL PRESSURE MONITORING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071505
510(k) Type
Traditional
Applicant
INTEGRA LIFESCIENCES CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/6/2007
Days to Decision
66 days
Submission Type
Summary