Cleared Traditional

Joimax Intracs System (K192663) - FDA 510(k) Clearance

Class II Orthopedic device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K192663 · Joimax GmbH · Orthopedic device
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Jul 2020
Decision
309d
Days
Class 2
Risk

K192663 is an FDA 510(k) clearance for the Joimax Intracs System. Classified as Orthopedic Stereotaxic Instrument within the OLO classification (a category covering orthopedic stereotaxic and surgical navigation instruments), Class II - Special Controls.

Submitted by Joimax GmbH (Karlsruhe, DE). The FDA issued a Cleared decision on July 30, 2020 after a review of 309 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 882.4560 - 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. Elevated predicate reliance profile. 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 Joimax GmbH devices

Submission Details

510(k) Number K192663 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 25, 2019
Decision Date July 30, 2020
Days to Decision 309 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
187d slower than avg
Panel avg: 122d · This submission: 309d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code OLO Orthopedic Stereotaxic Instrument
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 882.4560
Definition Stereotaxic Guidance During Orthopedic Surgery Procedures. Indicated For Orthopedic Joint Or Spine Surgery. Neurological Stereotaxic Instruments Are Classified Under Product Code Haw.
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 - OLO Orthopedic Stereotaxic Instrument

All 344
Devices cleared under the same product code (OLO) and FDA review panel - the closest regulatory comparables to K192663.
K2M Navigation Instruments
K201006 · K2m, Inc. · Aug 2020
CarboClear Navigated Instruments
K201251 · CarboFix Orthopedics , Ltd. · Aug 2020
Navigation Enabled Intruments
K200791 · Medos International SARL · Jul 2020
Mako Total Knee Application
K193515 · Mako Surgical Corp. · Jul 2020
ExcelsiusGPS Cranial 1.0 Module
K200047 · Globus Medical, Inc. · Jul 2020
OMNIBotics Knee System
K200888 · Corin, Ltd. · Jun 2020