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MODIFIED INS-1 INTRAOPERATIVE NERVE SURVEILLANCE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013215
510(k) Type
Special
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/2001
Days to Decision
20 days
Submission Type
Summary

MODIFIED INS-1 INTRAOPERATIVE NERVE SURVEILLANCE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013215
510(k) Type
Special
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/2001
Days to Decision
20 days
Submission Type
Summary