Last synced on 2 May 2025 at 11:05 pm

CoreLink Navigation Instruments

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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