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NuVasive Pulse System

Page Type
Cleared 510(K)
510(k) Number
K180038
510(k) Type
Traditional
Applicant
NuVasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/29/2018
Days to Decision
175 days
Submission Type
Summary

NuVasive Pulse System

Page Type
Cleared 510(K)
510(k) Number
K180038
510(k) Type
Traditional
Applicant
NuVasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/29/2018
Days to Decision
175 days
Submission Type
Summary