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“BioGend” Interbody Fusion System 001 Cage

Page Type
Cleared 510(K)
510(k) Number
K233075
510(k) Type
Traditional
Applicant
BioGend Therapeutics Co. Ltd.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
3/6/2024
Days to Decision
162 days
Submission Type
Summary

“BioGend” Interbody Fusion System 001 Cage

Page Type
Cleared 510(K)
510(k) Number
K233075
510(k) Type
Traditional
Applicant
BioGend Therapeutics Co. Ltd.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
3/6/2024
Days to Decision
162 days
Submission Type
Summary