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Rampart One Lumbar Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K191091
510(k) Type
Special
Applicant
Spineology, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/2019
Days to Decision
29 days
Submission Type
Summary

Rampart One Lumbar Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K191091
510(k) Type
Special
Applicant
Spineology, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/2019
Days to Decision
29 days
Submission Type
Summary