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SpineFrontier Lumbar Interbody Fusion Device System

Page Type
Cleared 510(K)
510(k) Number
K193106
510(k) Type
Special
Applicant
SpineFrontier, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/19/2020
Days to Decision
224 days
Submission Type
Summary

SpineFrontier Lumbar Interbody Fusion Device System

Page Type
Cleared 510(K)
510(k) Number
K193106
510(k) Type
Special
Applicant
SpineFrontier, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/19/2020
Days to Decision
224 days
Submission Type
Summary