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Standalone ALIF Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K221936
510(k) Type
Traditional
Applicant
Eminent Spine
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/2022
Days to Decision
108 days
Submission Type
Summary

Standalone ALIF Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K221936
510(k) Type
Traditional
Applicant
Eminent Spine
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/2022
Days to Decision
108 days
Submission Type
Summary