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SPINEFRONTIER PEDFUSE PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K133153
510(k) Type
Special
Applicant
SPINEFRONTIER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/14/2014
Days to Decision
209 days
Submission Type
Summary

SPINEFRONTIER PEDFUSE PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K133153
510(k) Type
Special
Applicant
SPINEFRONTIER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/14/2014
Days to Decision
209 days
Submission Type
Summary