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

Balanced Knee Revision System Trabecular Tibial Cone Augments

K Number: K182085 · Decision Oct 31, 2018
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
910
Applicant Total
14
Review Days
90

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Basic Information

Device Name
Balanced Knee Revision System Trabecular Tibial Cone Augments
K Number
K182085
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3560
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ortho Development Corporation
Date Received
August 2, 2018
Decision Date
October 31, 2018
Product Code
JWH
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
JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

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Other Clearances by Ortho Development Corporation

K Number Device Name
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K200281 The Gecko Spinal System
K181569 BKS Revision Sleeves System
K180743 Balanced Knee Revision System - Offset Junction Box
K173951 Legend Acetabular Liners
K171249 Entrada™ hip stem
K162995 Ibis® Pedicle Screw System
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