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Bundled Neurological Shunts and Accessories Product Families Labeling Modification to Support MR Conditional Labeling

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K153041
510(k) Type
Traditional
Applicant
Integra LifeSciences Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/14/2016
Days to Decision
147 days
Submission Type
Summary

Bundled Neurological Shunts and Accessories Product Families Labeling Modification to Support MR Conditional Labeling

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K153041
510(k) Type
Traditional
Applicant
Integra LifeSciences Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/14/2016
Days to Decision
147 days
Submission Type
Summary