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MODIFICATION TO NUVASIVE LATERAL PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K070273
510(k) Type
Special
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/2007
Days to Decision
64 days
Submission Type
Summary

MODIFICATION TO NUVASIVE LATERAL PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K070273
510(k) Type
Special
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/2007
Days to Decision
64 days
Submission Type
Summary