Cleared Traditional

K200823 - Zimmer, Inc. Hip Joint Prostheses MR Labeling I

K200823 is an FDA 510(k) clearance for Zimmer, manufactured by Zimmer, Inc.. The device is a Class 2 Orthopedic device with product code JDI cleared through the Traditional 510(k) pathway after a 101-day FDA review.

K200823 · Zimmer, Inc. · Orthopedic device
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Jul 2020
Decision
101d
Days
Class 2
Risk

K200823 is an FDA 510(k) clearance for the Zimmer, Inc. Hip Joint Prostheses MR Labeling I. Classified as Prosthesis, Hip, Semi-constrained, Metal/polymer, Cemented (product code JDI), Class II - Special Controls.

Submitted by Zimmer, Inc. (Warsaw, US). The FDA issued a Cleared decision on July 9, 2020 after a review of 101 days - within the typical 510(k) review window.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3350 - the FDA orthopedic device regulatory framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Orthopedic review framework, consistent with the majority of Class II 510(k) submissions.

View all Zimmer, Inc. devices

FDA 510(k) Submission Details - K200823

510(k) Number K200823 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 30, 2020
Decision Date July 09, 2020
Days to Decision 101 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
21d faster than avg
Panel avg: 122d · This submission: 101d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JDI Device Classification - Class 2, Special Controls

Product Code JDI Prosthesis, Hip, Semi-constrained, Metal/polymer, Cemented
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3350
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Orthopedic devices follow this clearance model.

Regulatory Peers - JDI Prosthesis, Hip, Semi-constrained, Metal/polymer, Cemented

All 514
Devices cleared under the same product code (JDI) and FDA review panel - the closest regulatory comparables to K200823.
PROFEMUR® GLADIATOR® Cemented Classic Stem
K201519 · Microport Orthopedics, Inc. · Dec 2020
Exeter V40 Femoral Stem, Exeter X3 RimFit Cup
K193429 · Howmedica Osteonics Corp. · Aug 2020
ZCA All-Poly Acetabular Cups
K191449 · Zimmer, Inc. · Jul 2020
CPT Hip System
K191735 · Zimmer, Inc. · Mar 2020
Conformity stem, cemented
K191056 · United Orthopedic Corporation · Jan 2020
EXETER Centralizer, EXETER 2.5mm Plug
K191414 · Stryker Orthopaedics · Aug 2019