FDA 510(k) Applications Submitted by Philippe Girard
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K172137 | 07/17/2017 | PIEZOTOME CUBE | Satelec - Acteon Group |
| K163610 | 12/22/2016 | PIEZOTOME M+, PIEZOTOME M+ Handpiece | SATALEC-ACTEON GROUP |
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