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SpineEX Sagittae Lateral Lumbar Interbody Fusion Devices

Page Type
Cleared 510(K)
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)
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