The following data is part of a premarket notification filed by Medicrea International S.a. with the FDA for Impix 3d Print Cages.
Device ID | K163595 |
510k Number | K163595 |
Device Name: | IMPIX 3D Print Cages |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
Applicant | MEDICREA INTERNATIONAL S.A. 5389 Route De Strasbourg Rillieux-la-pape, FR 69140 |
Contact | David Ryan |
Correspondent | David Ryan MEDICREA INTERNATIONAL S.A. 5389 Route De Strasbourg Rillieux-la-pape, FR 69140 |
Product Code | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-12-21 |
Decision Date | 2017-11-13 |
Summary: | summary |