The following data is part of a premarket notification filed by Medacta International Sa with the FDA for M.u.s.t. Mini Posterior Cervical Screws System.
Device ID | K171369 |
510k Number | K171369 |
Device Name: | M.U.S.T. MINI Posterior Cervical Screws System |
Classification | Posterior Cervical Screw System |
Applicant | Medacta International SA Strada Regina Castel San Pietro, CH Ch-6874 |
Contact | Stefano Baj |
Correspondent | Elizabeth Rose, Mst, Rac Mapi USA, Inc. 2343 Alexandria Drive Suite 100 Lexington, KY 40504 |
Product Code | NKG |
CFR Regulation Number | 888.3075 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-05-10 |
Decision Date | 2017-08-01 |
Summary: | summary |