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LATERAL VBR SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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