Last synced on 14 November 2025 at 11:06 pm

Renovis S141 Lumbar Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K170888
510(k) Type
Traditional
Applicant
Renovis Surgical Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2017
Days to Decision
134 days
Submission Type
Summary

Renovis S141 Lumbar Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K170888
510(k) Type
Traditional
Applicant
Renovis Surgical Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2017
Days to Decision
134 days
Submission Type
Summary