Skip to content
Scan

Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K213459

Glenoid Reconstruction System · Medacta International S.A. · decided 2022-11-23 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Glenoid Reconstruction System04.01.0303Medacta International SAPHX07630345710321
Glenoid Reconstruction System04.01.0320Medacta International SAPHX07630345710499
Glenoid Reconstruction System04.01.0300Medacta International SAPHX07630345710291
Glenoid Reconstruction System04.01.0311Medacta International SAPHX07630345710406
Glenoid Reconstruction System04.01.0302Medacta International SAPHX07630345710314
Glenoid Reconstruction System04.01.0321Medacta International SAPHX07630345710505
Glenoid Reconstruction System04.01.0304Medacta International SAPHX07630345710338
Glenoid Reconstruction System04.01.0301Medacta International SAPHX07630345710307
Glenoid Reconstruction System04.01.0310Medacta International SAPHX07630345710390
Glenoid Reconstruction System04.01.0307Medacta International SAPHX07630345710369
Glenoid Reconstruction System04.01.0306Medacta International SAPHX07630345710352
Glenoid Reconstruction System04.01.0323Medacta International SAPHX07630345710529
Glenoid Reconstruction System04.01.0322Medacta International SAPHX07630345710512
Glenoid Reconstruction System04.01.0305Medacta International SAPHX07630345710345
Glenoid Reconstruction System04.01.0308Medacta International SAPHX07630345710376
Glenoid Reconstruction System04.01.0309Medacta International SAPHX07630345710383