Cleared Traditional

K022199 - ENDIUS ATAVI SYSTEM

K022199 is the FDA 510(k) clearance for ENDIUS ATAVI SYSTEM by Endius, Inc.. It is a Class 2 Orthopedic device (product code HRX) cleared through the Traditional 510(k) pathway after a 89-day FDA review.

K022199 · Endius, Inc. · Orthopedic device
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Oct 2002
Decision
89d
Days
Class 2
Risk

K022199 is an FDA 510(k) clearance for the ENDIUS ATAVI SYSTEM. Classified as Arthroscope (product code HRX), Class II - Special Controls.

Submitted by Endius, Inc. (Plainville, US). The FDA issued a Cleared decision on October 2, 2002 after a review of 89 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.1100 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Endius, Inc. devices

Submission Details

510(k) Number K022199 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 05, 2002
Decision Date October 02, 2002
Days to Decision 89 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
33d faster than avg
Panel avg: 122d · This submission: 89d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code HRX Arthroscope
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.1100
Definition Validated Reprocessing Instructions And Reprocessing Validation Data For This Device Type Must Be Included In A 510(k) Submission If The Device Is Reusable And Has Specific Design Features (please Refer To Table 2 Of 82 Fr 26807, Available At Https://www.gpo.gov/fdsys/pkg/fr-2017-06-09/pdf/2017-12007.pdf).
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 - HRX Arthroscope

All 382
Devices cleared under the same product code (HRX) and FDA review panel - the closest regulatory comparables to K022199.
DYONICS POWER CONTROL UNIT
K030196 · Smith & Nephew, Inc. · Feb 2003
DAVOL ARTHROVENT OUTFLOW TUBING
K030307 · Davol, Inc. · Feb 2003
KSEA SPINOSCOPE
K023187 · Karl Storz Endoscopy · Dec 2002
ENDIUS FLEXTIP BLADE
K022578 · Endius, Inc. · Aug 2002
ENDIUS ATAVI SYSTEM
K021748 · Endius, Inc. · Jun 2002
POWER TEK II
K020761 · Biomet, Inc. · Apr 2002