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 |