Last synced on 25 January 2026 at 3:41 am

SSP PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060118
510(k) Type
Traditional
Applicant
Specialty Spine Products, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/2006
Days to Decision
142 days
Submission Type
Summary

SSP PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060118
510(k) Type
Traditional
Applicant
Specialty Spine Products, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/2006
Days to Decision
142 days
Submission Type
Summary