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INCITE INNOVATION STAND ALONE INTERBODY FUSION DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093808
510(k) Type
Traditional
Applicant
Incite Innovation, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/2010
Days to Decision
103 days
Submission Type
Summary

INCITE INNOVATION STAND ALONE INTERBODY FUSION DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093808
510(k) Type
Traditional
Applicant
Incite Innovation, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/2010
Days to Decision
103 days
Submission Type
Summary