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Opticage Expandable Interbody Fusion Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K152156
510(k) Type
Traditional
Applicant
Interventional Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/2015
Days to Decision
77 days
Submission Type
Statement

Opticage Expandable Interbody Fusion Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K152156
510(k) Type
Traditional
Applicant
Interventional Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/2015
Days to Decision
77 days
Submission Type
Statement