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Rubicon Lumbar Interbody Fusion System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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