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InFill Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K152259
510(k) Type
Traditional
Applicant
Pinnacle Spine Group, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/2015
Days to Decision
100 days
Submission Type
Summary

InFill Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K152259
510(k) Type
Traditional
Applicant
Pinnacle Spine Group, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/2015
Days to Decision
100 days
Submission Type
Summary