Last synced on 23 May 2025 at 11:06 pm

REFORM PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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