Last synced on 14 November 2025 at 11:06 pm

OPTICAGE INTERBODY FUSION DEVICE, MODEL SERIES 9070

Page Type
Cleared 510(K)
510(k) Number
K133583
510(k) Type
Special
Applicant
INTERVENTIONAL SPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/2014
Days to Decision
81 days
Submission Type
Summary

OPTICAGE INTERBODY FUSION DEVICE, MODEL SERIES 9070

Page Type
Cleared 510(K)
510(k) Number
K133583
510(k) Type
Special
Applicant
INTERVENTIONAL SPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/2014
Days to Decision
81 days
Submission Type
Summary