FDA 510(k) Applications Submitted by Merete GmbH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K181026 | 04/18/2018 | OsteoBridgeÖ IDSF System | Merete GmbH |
| K172213 | 07/24/2017 | MECRON Cannulated Screw System | Merete GmbH |
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