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

Page Type
Cleared 510(K)
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)
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