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Elite Expandable Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K162879
510(k) Type
Traditional
Applicant
Spineology Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/2017
Days to Decision
108 days
Submission Type
Summary

Elite Expandable Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K162879
510(k) Type
Traditional
Applicant
Spineology Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/2017
Days to Decision
108 days
Submission Type
Summary