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NUVASIVE LATERAL PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K091071
510(k) Type
Special
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/2009
Days to Decision
24 days
Submission Type
Summary

NUVASIVE LATERAL PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K091071
510(k) Type
Special
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/2009
Days to Decision
24 days
Submission Type
Summary