The following data is part of a premarket notification filed by Limacorporate S.p.a. with the FDA for Tema Elbow System.
| Device ID | K181362 |
| 510k Number | K181362 |
| Device Name: | TEMA Elbow System |
| Classification | Prosthesis, Elbow, Constrained, Cemented |
| Applicant | Limacorporate S.p.A. via Nazionale 52 Villanova Di San Daniele, IT 33038 |
| Contact | Roberto Gabetta |
| Correspondent | Stephen Peoples Peoples & Associates Consulting LLC 5010 Lodge Pole Lane Fort Wayne, IN 46814 |
| Product Code | JDC |
| CFR Regulation Number | 888.3150 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-05-23 |
| Decision Date | 2019-02-16 |
| Summary: | summary |