FDA 510(k) Applications Submitted by Megan Bernier
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K210167 | 01/21/2021 | DELTA XTEND Reverse Shoulder System | DePuy Orthopaedics Inc. |
| K203230 | 11/02/2020 | Global Shoulder and Delta CTA systems | DePuy lnc. |
| K163435 | 12/07/2016 | Entellus Medical Reinforced Anesthesia Needle | Entellus Medical Inc. |
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