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

MPO Hip Instruments

K Number: K213816 · Decision Jan 5, 2022
Classifications
1
FEI Numbers
227
Registration Numbers
227
Same Product Code
562
Applicant Total
37
Review Days
29

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Basic Information

Device Name
MPO Hip Instruments
K Number
K213816
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3350
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Microport Orthopedics, Inc.
Date Received
December 7, 2021
Decision Date
January 5, 2022
Product Code
JDI
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
JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

Similar 510(k) Clearances

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Other Clearances by Microport Orthopedics, Inc.

K Number Device Name
K250444 NEXUS® Hip Stem
K243574 Evolution® Total Knee Systems - Kinematic Alignment Instrumentation and Technique
K240452 Ceramic Femoral Head
K240043 EVOLUTION® Hinge Knee System;GUARDIAN™ limb Salvage System;DCW Modular Distal Femoral System;REPIPHYSIS™ Limb Salvage System;EVOLUTION® MP Total Knee System; EVOLUTION® MP Total Knee System; EVOLUTION® MP Adaptive CS Insert; EVOLUTION® MP Adaptive PS Tibial Insert; EVOLUTION® MP CS/CR Porous Femur/EVOLUTION® Adaptive CS and PS Inserts; EVOLUTION® Revision CCK System; ADVANCE® Double High Insert; ADVANCE® A-CLASS® Tibial Insert; ADVANCE® Knee System; ADVANCE® Ultra-Congruent Tibial Inse
K233507 EVOLUTION® Tibial Cones
K231947 EVOLUTION® Cement Keel
K230563 EVOLUTION® Hinge Knee System
K213817 MPO Knee Instruments; MPO PROPHECY Knee Instruments
K200011 E-CLASS® DUAL MOBILITY INSERTS and DYNASTY® DUAL MOBILITY LINERS
K201157 Prime BIOFOAM® Multi-Hole Shells
Search all 37 clearances from Microport Orthopedics, Inc. →