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TDM Lumbar Interbody Fusion Cage System

Page Type
Cleared 510(K)
510(k) Number
K221844
510(k) Type
Traditional
Applicant
TDM Co., Ltd
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
8/17/2022
Days to Decision
54 days
Submission Type
Summary

TDM Lumbar Interbody Fusion Cage System

Page Type
Cleared 510(K)
510(k) Number
K221844
510(k) Type
Traditional
Applicant
TDM Co., Ltd
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
8/17/2022
Days to Decision
54 days
Submission Type
Summary