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Rampart A Lumbar Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K153082
510(k) Type
Traditional
Applicant
SPINEOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/2016
Days to Decision
104 days
Submission Type
Summary

Rampart A Lumbar Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K153082
510(k) Type
Traditional
Applicant
SPINEOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/2016
Days to Decision
104 days
Submission Type
Summary