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ZSFab Lumbar Interbody System

Page Type
Cleared 510(K)
510(k) Number
K221858
510(k) Type
Traditional
Applicant
ZS Fab Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/14/2022
Days to Decision
109 days
Submission Type
Summary

ZSFab Lumbar Interbody System

Page Type
Cleared 510(K)
510(k) Number
K221858
510(k) Type
Traditional
Applicant
ZS Fab Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/14/2022
Days to Decision
109 days
Submission Type
Summary