FDA 510(k) Applications Submitted by SINTEA PLASTEK, LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K101886 | 07/06/2010 | DSC/ALF SPINAL SYSTEM | SINTEA PLASTEK, LLC |
| K112611 | 09/07/2011 | SINTEA PLUSTEK PLS MULTI-AXIAL SCREWS | SINTEA PLASTEK, LLC |
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