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Republic Spine Restore Cervical Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K190889
510(k) Type
Traditional
Applicant
Republic Spine, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/19/2019
Days to Decision
75 days
Submission Type
Summary

Republic Spine Restore Cervical Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K190889
510(k) Type
Traditional
Applicant
Republic Spine, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/19/2019
Days to Decision
75 days
Submission Type
Summary