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OPTICAGE INTERBODY FUSION DEVICE, MODEL SERIES 9070

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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