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Duo Lumbar Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K171660
510(k) Type
Special
Applicant
Spineology Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/2017
Days to Decision
74 days
Submission Type
Summary

Duo Lumbar Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K171660
510(k) Type
Special
Applicant
Spineology Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/2017
Days to Decision
74 days
Submission Type
Summary