Last synced on 14 November 2025 at 11:06 pm

Foundation 3D Interbody

Page Type
Cleared 510(K)
510(k) Number
K162496
510(k) Type
Traditional
Applicant
CoreLink, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/2017
Days to Decision
239 days
Submission Type
Summary

Foundation 3D Interbody

Page Type
Cleared 510(K)
510(k) Number
K162496
510(k) Type
Traditional
Applicant
CoreLink, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/2017
Days to Decision
239 days
Submission Type
Summary