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InFill Interbody Fusion Devices

Page Type
Cleared 510(K)
510(k) Number
K151184
510(k) Type
Traditional
Applicant
PINNACLE SPINE GROUP, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/2015
Days to Decision
71 days
Submission Type
Summary

InFill Interbody Fusion Devices

Page Type
Cleared 510(K)
510(k) Number
K151184
510(k) Type
Traditional
Applicant
PINNACLE SPINE GROUP, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/2015
Days to Decision
71 days
Submission Type
Summary