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NUVASIVE COROENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K081611
510(k) Type
Traditional
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/2/2008
Days to Decision
115 days
Submission Type
Summary

NUVASIVE COROENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K081611
510(k) Type
Traditional
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/2/2008
Days to Decision
115 days
Submission Type
Summary