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NextGen Pedicle Screw System

Page Type
Cleared 510(K)
510(k) Number
K221776
510(k) Type
Traditional
Applicant
CoreLink, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/2022
Days to Decision
49 days
Submission Type
Summary

NextGen Pedicle Screw System

Page Type
Cleared 510(K)
510(k) Number
K221776
510(k) Type
Traditional
Applicant
CoreLink, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/2022
Days to Decision
49 days
Submission Type
Summary