The following data is part of a premarket notification filed by Clariance, Sa with the FDA for Idys-c Zp 3dti.
| Device ID | K212562 |
| 510k Number | K212562 |
| Device Name: | Idys-C ZP 3DTi |
| Classification | Intervertebral Fusion Device With Integrated Fixation, Cervical |
| Applicant | Clariance, SA 18, Rue Robespierre Beaurains, FR 62217 |
| Contact | Mélody La Porte |
| Correspondent | Janice M. Hogan Hogan Lovells US LLP 1735 Market Street, 23rd Floor Philadelphia, PA 19103 |
| Product Code | OVE |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2021-08-13 |
| Decision Date | 2021-10-12 |
| Summary: | summary |