Cleared Traditional

K951847 - AVANTGARDE

K951847 is an FDA 510(k) clearance for AVANTGARDE, manufactured by Otto Bock Orthopedic Industry, Inc.. The device is a Class 1 Physical Medicine device with product code IOR cleared through the Traditional 510(k) pathway after a 22-day FDA review.

K951847 · Otto Bock Orthopedic Industry, Inc. · Physical Medicine device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
May 1995
Decision
22d
Days
Class 1
Risk

K951847 is an FDA 510(k) clearance for the AVANTGARDE. Classified as Wheelchair, Mechanical (product code IOR), Class I - General Controls.

Submitted by Otto Bock Orthopedic Industry, Inc. (Plymouth, US). The FDA issued a Cleared decision on May 12, 1995 after a review of 22 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.3850 - the FDA physical medicine device 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.

FDA 510(k) Submission Details - K951847

510(k) Number K951847 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 20, 1995
Decision Date May 12, 1995
Days to Decision 22 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
94d faster than avg
Panel avg: 116d · This submission: 22d
Pathway characteristics
Predicate-based equivalence.

IOR Device Classification - Class 1, General Controls

Product Code IOR Wheelchair, Mechanical
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 890.3850
Definition A Mechanical Wheelchair Is A Manually Operated Device With Wheels That Is Intended For Medical Purposes To Provide Mobility To Persons Restricted To A Sitting Position. Fda Interprets “mobility To Persons Restricted To A Sitting Position” To Mean The Device Type Is Intended To Provide Mobility To Individuals Who Have Mobility Impairments And/or Require An Assistive Device For Mobility.
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - IOR Wheelchair, Mechanical

All 466
Devices cleared under the same product code (IOR) and FDA review panel - the closest regulatory comparables to K951847.
MECHANICAL WHEELCHAIR- LIL DIPPER
K945153 · Colours 'N Motion · May 1995
MECHANICAL WHEELCHAIR 890.3850
K945175 · Lumex, Inc. · May 1995
CHAMPION
K950815 · Kleinfeld, Kaplan and Becker · May 1995
MECHANICAL WHEELCHAIR- IMPACT
K945152 · Colours 'N Motion · May 1995
X2000 TRADITIONAL WHEELCHAIR
K951351 · Homecrest Industries · Apr 1995
RADIUS MANUAL WHWWLCHAIRS (COBRA, VIPER, SWING, OLYMPIA, AND MOBIL MODELS)
K951560 · Radius Intl., Inc. · Apr 1995
K951847 · AVANTGARDE
Download PDF FDA Summary Otto Bock Orthopedic …