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restor3d TiDAL Lumbar Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K220523
510(k) Type
Traditional
Applicant
Restor3d
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/2022
Days to Decision
114 days
Submission Type
Summary

restor3d TiDAL Lumbar Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K220523
510(k) Type
Traditional
Applicant
Restor3d
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/2022
Days to Decision
114 days
Submission Type
Summary