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Ti-Largo Cervical Interbody System

Page Type
Cleared 510(K)
510(k) Number
K223231
510(k) Type
Traditional
Applicant
FloSpine
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/2023
Days to Decision
129 days
Submission Type
Summary

Ti-Largo Cervical Interbody System

Page Type
Cleared 510(K)
510(k) Number
K223231
510(k) Type
Traditional
Applicant
FloSpine
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/2023
Days to Decision
129 days
Submission Type
Summary