Biomet Manufacturing Corp
FDA 510(k) & PMA Approved Dispositivos — 15 products
Publicidade
Total de dispositivos15
Categorias0
Última decisão da FDA
| Tipo | Número | Nome do dispositivo | Código | Data | Ações |
|---|---|---|---|---|---|
| 510(k) | K230540 | Patient Specific Planning Solution™ 3D Bone Models | LLZ | 2023-07-25 | Ver |
| 510(k) | K214001 | Comprehensive® Shoulder System, Comprehensive® Reverse Shoulder System | PHX | 2023-03-15 | Ver |
| 510(k) | K211729 | Comprehensive® Convertible Glenoid - Vivacit-E Liner | PHX | 2021-11-04 | Ver |
| 510(k) | K202232 | Comprehensive Vault Reconstruction System | PHX | 2021-02-19 | Ver |
| 510(k) | K193038 | Comprehensive Shoulder System | MBF | 2020-10-28 | Ver |
| 510(k) | K182516 | Comprehensive Nano Stemless Shoulder | PKC | 2019-04-22 | Ver |
| 510(k) | K181611 | Comprehensive Reverse Shoulder System | PHX | 2018-09-24 | Ver |
| 510(k) | K173411 | Comprehensive Segmental Revision System (SRS) | PHX | 2018-02-08 | Ver |
| 510(k) | K172502 | Comprehensive Augmented Glenoid Components, Comprehensive Standard Baseplate, Comprehensive Mini Baseplate | PHX | 2018-01-03 | Ver |
| 510(k) | K163651 | ExpressBraid Graft Manipulation | GAT | 2017-02-17 | Ver |
| 510(k) | K152754 | COMPREHENSIVE VAULT RECONSTRUCTION SYSTEM (VRS) | PHX | 2016-05-16 | Ver |
| 510(k) | K153558 | Ventix Suture Anchor | MBI | 2016-04-21 | Ver |
| 510(k) | K152262 | Ventix Knotless Anchors | MBI | 2016-03-08 | Ver |
| 510(k) | K152868 | ExpressBraid Graft Manipulation | GAT | 2016-02-08 | Ver |
| 510(k) | K153398 | Comprehensive SRS/Nexel Elbow | JDC | 2016-02-03 | Ver |
Nenhum dispositivo correspondente.