Last synced on 25 April 2025 at 11:05 pm

“BioGend” Interbody Fusion System 001 Cage

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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