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Opticage(R) Expandable Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K160464
510(k) Type
Special
Applicant
INTERVENTIONAL SPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/2016
Days to Decision
45 days
Submission Type
Summary

Opticage(R) Expandable Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K160464
510(k) Type
Special
Applicant
INTERVENTIONAL SPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/2016
Days to Decision
45 days
Submission Type
Summary