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GAIA Lumbar Interbody Fusion Device (LIFD) Family

Page Type
Cleared 510(K)
510(k) Number
K201939
510(k) Type
Traditional
Applicant
PrinterPrezz
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/8/2020
Days to Decision
87 days
Submission Type
Summary

GAIA Lumbar Interbody Fusion Device (LIFD) Family

Page Type
Cleared 510(K)
510(k) Number
K201939
510(k) Type
Traditional
Applicant
PrinterPrezz
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/8/2020
Days to Decision
87 days
Submission Type
Summary