FDA 510(k) Applications Submitted by Aesculap Implants Systems, LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K143443 | 12/02/2014 | VEGA Knee System, Columbus Total Knee System | Aesculap Implants Systems, LLC |
| K172235 | 07/25/2017 | CoreHip« System | Aesculap Implants Systems, LLC |
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