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 |