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OPTICAGE INTERBODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K113527
510(k) Type
Traditional
Applicant
INTERVENTIONAL SPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/20/2012
Days to Decision
51 days
Submission Type
Summary

OPTICAGE INTERBODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K113527
510(k) Type
Traditional
Applicant
INTERVENTIONAL SPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/20/2012
Days to Decision
51 days
Submission Type
Summary