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DIGITAL LIGHTBOX

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093117
510(k) Type
Traditional
Applicant
Brainlab AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
12/11/2009
Days to Decision
70 days
Submission Type
Summary

DIGITAL LIGHTBOX

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093117
510(k) Type
Traditional
Applicant
Brainlab AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
12/11/2009
Days to Decision
70 days
Submission Type
Summary