Last synced on 14 November 2025 at 11:06 pm

REFORM PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K131343
510(k) Type
Traditional
Applicant
SPINAL USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/24/2013
Days to Decision
76 days
Submission Type
Summary

REFORM PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K131343
510(k) Type
Traditional
Applicant
SPINAL USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/24/2013
Days to Decision
76 days
Submission Type
Summary