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Duo Lumbar Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K190055
510(k) Type
Special
Applicant
Spineology Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/2019
Days to Decision
55 days
Submission Type
Summary

Duo Lumbar Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K190055
510(k) Type
Special
Applicant
Spineology Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/2019
Days to Decision
55 days
Submission Type
Summary