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NUVASIVE EMG ENDOTRACHEAL TUBE

Page Type
Cleared 510(K)
510(k) Number
K133530
510(k) Type
Traditional
Applicant
NUVASIVE, INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/2014
Days to Decision
168 days
Submission Type
Summary

NUVASIVE EMG ENDOTRACHEAL TUBE

Page Type
Cleared 510(K)
510(k) Number
K133530
510(k) Type
Traditional
Applicant
NUVASIVE, INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/2014
Days to Decision
168 days
Submission Type
Summary