Biomet Manufacturing Corp - FDA 510(k) Cleared Devices
Recent clearances: Patient Specific Planning Solution™ 3D Bone Models, Comprehensive® Shoulder System, Comprehensive® Reverse Shoulder System, Comprehensive® Convertible Glenoid - Vivacit-E Liner
93
Total
93
Cleared
0
Denied
FDA 510(k) Regulatory Record - Biomet Manufacturing Corp Orthopedic ✕
87 devices
Cleared
Mar 15, 2023
Comprehensive® Shoulder System, Comprehensive® Reverse Shoulder System
Orthopedic
449d
Cleared
Nov 04, 2021
Comprehensive® Convertible Glenoid - Vivacit-E Liner
Orthopedic
153d
Cleared
Feb 19, 2021
Comprehensive Vault Reconstruction System
Orthopedic
196d
Cleared
Oct 28, 2020
Comprehensive Shoulder System
Orthopedic
363d
Cleared
CT
Apr 22, 2019
Comprehensive Nano Stemless Shoulder
Orthopedic
221d
Cleared
Sep 24, 2018
Comprehensive Reverse Shoulder System
Orthopedic
97d
Cleared
Feb 08, 2018
Comprehensive Segmental Revision System (SRS)
Orthopedic
99d
Cleared
Jan 03, 2018
Comprehensive Augmented Glenoid Components, Comprehensive Standard Baseplate,...
Orthopedic
138d
Cleared
May 16, 2016
COMPREHENSIVE VAULT RECONSTRUCTION SYSTEM (VRS)
Orthopedic
235d
Cleared
Apr 21, 2016
Ventix Suture Anchor
Orthopedic
129d
Cleared
Mar 08, 2016
Ventix Knotless Anchors
Orthopedic
210d
Cleared
Feb 03, 2016
Comprehensive SRS/Nexel Elbow
Orthopedic
71d
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