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SPINEFRONTIER PEDFUSE PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K123164
510(k) Type
Traditional
Applicant
SPINEFRONTIER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/15/2013
Days to Decision
129 days
Submission Type
Summary

SPINEFRONTIER PEDFUSE PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K123164
510(k) Type
Traditional
Applicant
SPINEFRONTIER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/15/2013
Days to Decision
129 days
Submission Type
Summary