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LATERAL VBR SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K140563
510(k) Type
Traditional
Applicant
NUVASIVE, INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/2014
Days to Decision
155 days
Submission Type
Statement

LATERAL VBR SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K140563
510(k) Type
Traditional
Applicant
NUVASIVE, INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/2014
Days to Decision
155 days
Submission Type
Statement