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Eminent Spine 3D Lumbar Interbody Fusion Systems

Page Type
Cleared 510(K)
510(k) Number
K230219
510(k) Type
Traditional
Applicant
Eminent Spine, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/16/2023
Days to Decision
110 days
Submission Type
Summary

Eminent Spine 3D Lumbar Interbody Fusion Systems

Page Type
Cleared 510(K)
510(k) Number
K230219
510(k) Type
Traditional
Applicant
Eminent Spine, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/16/2023
Days to Decision
110 days
Submission Type
Summary