Last synced on 13 May 2022 at 11:05 pm

NUVASIVE 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
K002677
510(k) Type
Traditional
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/2000
Days to Decision
77 days
Submission Type
Summary

NUVASIVE 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
K002677
510(k) Type
Traditional
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/2000
Days to Decision
77 days
Submission Type
Summary