The following data is part of a premarket notification filed by Medacta International with the FDA for M.u.s.t Pedicle Screw System.
| Device ID | K141988 |
| 510k Number | K141988 |
| Device Name: | M.U.S.T PEDICLE SCREW SYSTEM |
| Classification | Thoracolumbosacral Pedicle Screw System |
| Applicant | MEDACTA INTERNATIONAL 1556 W. CARROLL AVENUE Chicago, IL 60607 |
| Contact | Adam Gross |
| Correspondent | Adam Gross MEDACTA INTERNATIONAL 1556 W. CARROLL AVENUE Chicago, IL 60607 |
| Product Code | NKB |
| Subsequent Product Code | KWP |
| Subsequent Product Code | KWQ |
| Subsequent Product Code | MNH |
| Subsequent Product Code | MNI |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-07-22 |
| Decision Date | 2014-08-19 |
| Summary: | summary |