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proGAV Programmable Shunt System, proGAV 2.0 Adjustable Shunt System, proSA Adjustable Shunt System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161853
510(k) Type
Traditional
Applicant
AESCULAP INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/2017
Days to Decision
236 days
Submission Type
Summary

proGAV Programmable Shunt System, proGAV 2.0 Adjustable Shunt System, proSA Adjustable Shunt System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161853
510(k) Type
Traditional
Applicant
AESCULAP INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/2017
Days to Decision
236 days
Submission Type
Summary