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NUVASIVE ANTERIOR LUMBAR PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K072339
510(k) Type
Special
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/2007
Days to Decision
60 days
Submission Type
Summary

NUVASIVE ANTERIOR LUMBAR PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K072339
510(k) Type
Special
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/2007
Days to Decision
60 days
Submission Type
Summary