Cleared Traditional

K051861 - THE SAVION INDUSTRIES MEDI-CRUISER MODEL MS777

K051861 is an FDA 510(k) clearance for THE SAVION INDUSTRIES MEDI-CRUISER MODE..., manufactured by Savion Industries, Ltd.. The device is a Class 2 Physical Medicine device with product code INK cleared through the Traditional 510(k) pathway after a 83-day FDA review.

K051861 · Savion Industries, Ltd. · Physical Medicine device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Sep 2005
Decision
83d
Days
Class 2
Risk

K051861 is an FDA 510(k) clearance for the THE SAVION INDUSTRIES MEDI-CRUISER MODEL MS777. Classified as Stretcher, Wheeled, Powered (product code INK), Class II - Special Controls.

Submitted by Savion Industries, Ltd. (Ashdod, IL). The FDA issued a Cleared decision on September 28, 2005 after a review of 83 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.3690 - 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.

View all Savion Industries, Ltd. devices

FDA 510(k) Submission Details - K051861

510(k) Number K051861 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 07, 2005
Decision Date September 28, 2005
Days to Decision 83 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
32d faster than avg
Panel avg: 115d · This submission: 83d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

INK Device Classification - Class 2, Special Controls

Product Code INK Stretcher, Wheeled, Powered
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 890.3690
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 Physical Medicine devices follow this clearance model.

Regulatory Peers - INK Stretcher, Wheeled, Powered

Devices cleared under the same product code (INK) and FDA review panel - the closest regulatory comparables to K051861.
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