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SpineFrontier Lumbar Interbody Fusion Device System

Page Type
Cleared 510(K)
510(k) Number
K142504
510(k) Type
Traditional
Applicant
SpineFrontier, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/2015
Days to Decision
250 days
Submission Type
Summary

SpineFrontier Lumbar Interbody Fusion Device System

Page Type
Cleared 510(K)
510(k) Number
K142504
510(k) Type
Traditional
Applicant
SpineFrontier, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/2015
Days to Decision
250 days
Submission Type
Summary