FDA 510(k) Applications Submitted by Robert Lange
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K181963 | 07/23/2018 | ostaPek Interbody Fusion Cages | coLigne, AG |
| K173148 | 09/29/2017 | ACIF | coLigne, AG |
| K173893 | 12/21/2017 | Trabis | coLigne, AG |
| K210306 | 02/03/2021 | GII Spinal Fixation System | Coligne AG |
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