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S 100 PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K111940
510(k) Type
Special
Applicant
Renovis Surgical Technologies, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/2012
Days to Decision
312 days
Submission Type
Summary

S 100 PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K111940
510(k) Type
Special
Applicant
Renovis Surgical Technologies, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/2012
Days to Decision
312 days
Submission Type
Summary