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Lumbar Interbody Fusion System (OLLIF)

Page Type
Cleared 510(K)
510(k) Number
K173947
510(k) Type
Traditional
Applicant
Advanced Research Medical, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/2018
Days to Decision
210 days
Submission Type
Summary

Lumbar Interbody Fusion System (OLLIF)

Page Type
Cleared 510(K)
510(k) Number
K173947
510(k) Type
Traditional
Applicant
Advanced Research Medical, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/2018
Days to Decision
210 days
Submission Type
Summary