Last synced on 14 November 2025 at 11:06 pm

CoreLink Navigation Instruments

Page Type
Cleared 510(K)
510(k) Number
K212825
510(k) Type
Traditional
Applicant
CoreLink, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/13/2021
Days to Decision
40 days
Submission Type
Summary

CoreLink Navigation Instruments

Page Type
Cleared 510(K)
510(k) Number
K212825
510(k) Type
Traditional
Applicant
CoreLink, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/13/2021
Days to Decision
40 days
Submission Type
Summary