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Opticage Expandable Interbody Fusion Device

Page Type
Cleared 510(K)
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)
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