Last synced on 27 June 2025 at 11:06 pm

LANCER PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110633
510(k) Type
Special
Applicant
SPINAL SOLUTIONS, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/15/2011
Days to Decision
286 days
Submission Type
Summary

LANCER PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110633
510(k) Type
Special
Applicant
SPINAL SOLUTIONS, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/15/2011
Days to Decision
286 days
Submission Type
Summary