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 |