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Rubicon Lumbar Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K181030
510(k) Type
Traditional
Applicant
Rubicon Spine, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/2018
Days to Decision
90 days
Submission Type
Summary

Rubicon Lumbar Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K181030
510(k) Type
Traditional
Applicant
Rubicon Spine, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/2018
Days to Decision
90 days
Submission Type
Summary