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NUVASIVE LATERAL PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K082070
510(k) Type
Special
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/24/2008
Days to Decision
64 days
Submission Type
Summary

NUVASIVE LATERAL PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K082070
510(k) Type
Special
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/24/2008
Days to Decision
64 days
Submission Type
Summary