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Renovis S180 Lateral Lumbar Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K181655
510(k) Type
Traditional
Applicant
Renovis Surgical Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/2018
Days to Decision
81 days
Submission Type
Summary

Renovis S180 Lateral Lumbar Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K181655
510(k) Type
Traditional
Applicant
Renovis Surgical Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/2018
Days to Decision
81 days
Submission Type
Summary