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NuVasive® Lumbar Interbody Implants

Page Type
Cleared 510(K)
510(k) Number
K153782
510(k) Type
Traditional
Applicant
NUVASIVE, INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/2016
Days to Decision
84 days
Submission Type
Summary

NuVasive® Lumbar Interbody Implants

Page Type
Cleared 510(K)
510(k) Number
K153782
510(k) Type
Traditional
Applicant
NUVASIVE, INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/2016
Days to Decision
84 days
Submission Type
Summary