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Spine Innovation Interbody System

Page Type
Cleared 510(K)
510(k) Number
K153356
510(k) Type
Traditional
Applicant
Spine Innovation LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/14/2016
Days to Decision
55 days
Submission Type
Summary

Spine Innovation Interbody System

Page Type
Cleared 510(K)
510(k) Number
K153356
510(k) Type
Traditional
Applicant
Spine Innovation LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/14/2016
Days to Decision
55 days
Submission Type
Summary