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Duo™ Lumbar Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K181792
510(k) Type
Special
Applicant
Spineology Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/2018
Days to Decision
40 days
Submission Type
Summary

Duo™ Lumbar Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K181792
510(k) Type
Special
Applicant
Spineology Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/2018
Days to Decision
40 days
Submission Type
Summary