FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Comprehensive® Convertible Glenoid - Vivacit-E Liner

K Number: K211729 · Decision Nov 4, 2021
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
203
Applicant Total
93
Review Days
153

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Basic Information

Device Name
Comprehensive® Convertible Glenoid - Vivacit-E Liner
K Number
K211729
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3660
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biomet Manufacturing Corp
Date Received
June 4, 2021
Decision Date
November 4, 2021
Product Code
PHX
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
PHX Shoulder Prosthesis, Reverse Configuration

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K Number Device Name
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K202232 Comprehensive Vault Reconstruction System
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K182516 Comprehensive Nano Stemless Shoulder
K181611 Comprehensive Reverse Shoulder System
K173411 Comprehensive Segmental Revision System (SRS)
K172502 Comprehensive Augmented Glenoid Components, Comprehensive Standard Baseplate, Comprehensive Mini Baseplate
K163651 ExpressBraid Graft Manipulation
K152754 COMPREHENSIVE VAULT RECONSTRUCTION SYSTEM (VRS)
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