The following data is part of a premarket notification filed by Medacta International Sa with the FDA for Mecta-c With Titanium Markers And Mecta-c Tipeek With Titanium Markers.
Device ID | K172587 |
510k Number | K172587 |
Device Name: | Mecta-C With Titanium Markers And Mecta-C TiPEEK With Titanium Markers |
Classification | Intervertebral Fusion Device With Bone Graft, Cervical |
Applicant | Medacta International SA Strada Regina Castel San Pietro, CH Ch-6874 |
Contact | Stefano Baj |
Correspondent | Elizabeth Rose, Mst, Rac (us) Mapi USA, Inc. 2343 Alexandria Drive, Suite 100 Lexington, KY 40504 |
Product Code | ODP |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-08-28 |
Decision Date | 2017-09-18 |
Summary: | summary |