FDA 510(k) Applications Submitted by NEOORTHO PRODUCTOS ORTHOPEDICOS S/A
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K142419 | 08/28/2014 | Mini and Micro Fragments Reconstruction System-NEOFIX | NEOORTHO PRODUCTOS ORTHOPEDICOS S/A |
| K132653 | 08/26/2013 | NEOPLATE SPINE ANTERIOR FIXATION SYSTEM | NEOORTHO PRODUCTOS ORTHOPEDICOS S/A |
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