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SpineEX Sagittae Lateral Lumbar Interbody Fusion Devices

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K200816
510(k) Type
Special
Applicant
Spineex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/2020
Days to Decision
31 days
Submission Type
Summary

SpineEX Sagittae Lateral Lumbar Interbody Fusion Devices

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K200816
510(k) Type
Special
Applicant
Spineex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/2020
Days to Decision
31 days
Submission Type
Summary