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Gemini-C Hybrid Cervical Interbody System

Page Type
Cleared 510(K)
510(k) Number
K170844
510(k) Type
Traditional
Applicant
Osseus Fusion Systems, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/3/2017
Days to Decision
104 days
Submission Type
Summary

Gemini-C Hybrid Cervical Interbody System

Page Type
Cleared 510(K)
510(k) Number
K170844
510(k) Type
Traditional
Applicant
Osseus Fusion Systems, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/3/2017
Days to Decision
104 days
Submission Type
Summary