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MODIFCATION TO: NUVASIVE NEUROVISION EMG ENDOTRACHEAL TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K094054
510(k) Type
Special
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/14/2010
Days to Decision
134 days
Submission Type
Summary

MODIFCATION TO: NUVASIVE NEUROVISION EMG ENDOTRACHEAL TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K094054
510(k) Type
Special
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/14/2010
Days to Decision
134 days
Submission Type
Summary