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OPTICAGE EXPANDABLE INTERBODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K140716
510(k) Type
Traditional
Applicant
INTERVENTIONAL SPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/24/2014
Days to Decision
248 days
Submission Type
Summary

OPTICAGE EXPANDABLE INTERBODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K140716
510(k) Type
Traditional
Applicant
INTERVENTIONAL SPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/24/2014
Days to Decision
248 days
Submission Type
Summary