The following data is part of a premarket notification filed by Limacorporate S.p.a. with the FDA for Limacorporate Smr Reverse Shoulder System.
| Device ID | K113523 |
| 510k Number | K113523 |
| Device Name: | LIMACORPORATE SMR REVERSE SHOULDER SYSTEM |
| Classification | Shoulder Prosthesis, Reverse Configuration |
| Applicant | LIMACORPORATE S.P.A. P.O. BOX 696 Winona Lake, IN 46590 -696 |
| Contact | Cheryl Hastings |
| Correspondent | Cheryl Hastings LIMACORPORATE S.P.A. P.O. BOX 696 Winona Lake, IN 46590 -696 |
| Product Code | PHX |
| CFR Regulation Number | 888.3660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-11-29 |
| Decision Date | 2011-12-20 |
| Summary: | summary |