Last synced on 14 November 2025 at 11:06 pm

Rampart One Lumbar Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K163670
510(k) Type
Traditional
Applicant
SPINEOLOGY INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/2017
Days to Decision
132 days
Submission Type
Summary

Rampart One Lumbar Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K163670
510(k) Type
Traditional
Applicant
SPINEOLOGY INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/2017
Days to Decision
132 days
Submission Type
Summary