Last synced on 14 November 2025 at 11:06 pm

CoreLink Navigation Instruments

Page Type
Cleared 510(K)
510(k) Number
K214059
510(k) Type
Special
Applicant
CoreLink, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/2022
Days to Decision
23 days
Submission Type
Summary

CoreLink Navigation Instruments

Page Type
Cleared 510(K)
510(k) Number
K214059
510(k) Type
Special
Applicant
CoreLink, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/2022
Days to Decision
23 days
Submission Type
Summary