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NUVASIVE SAGE LATERAL PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K121815
510(k) Type
Traditional
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/23/2012
Days to Decision
125 days
Submission Type
Summary

NUVASIVE SAGE LATERAL PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K121815
510(k) Type
Traditional
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/23/2012
Days to Decision
125 days
Submission Type
Summary