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CoreLink Robotic Navigation Instruments

Page Type
Cleared 510(K)
510(k) Number
K231494
510(k) Type
Traditional
Applicant
Corelink, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/27/2023
Days to Decision
157 days
Submission Type
Summary

CoreLink Robotic Navigation Instruments

Page Type
Cleared 510(K)
510(k) Number
K231494
510(k) Type
Traditional
Applicant
Corelink, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/27/2023
Days to Decision
157 days
Submission Type
Summary