Cleared Traditional

K152474 - Avitus Bone Harvester

K152474 is an FDA 510(k) clearance for Avitus Bone Harvester, manufactured by Avitus Orthopaedics, Inc.. The device is a Class 2 Gastroenterology & Urology device with product code KNW cleared through the Traditional 510(k) pathway after a 53-day FDA review.

K152474 · Avitus Orthopaedics, Inc. · Gastroenterology & Urology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Oct 2015
Decision
53d
Days
Class 2
Risk

K152474 is an FDA 510(k) clearance for the Avitus Bone Harvester. Classified as Instrument, Biopsy (product code KNW), Class II - Special Controls.

Submitted by Avitus Orthopaedics, Inc. (Farmington, US). The FDA issued a Cleared decision on October 23, 2015 after a review of 53 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.1075 - the FDA gastroenterology and urology 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 Avitus Orthopaedics, Inc. devices

FDA 510(k) Submission Details - K152474

510(k) Number K152474 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 31, 2015
Decision Date October 23, 2015
Days to Decision 53 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
78d faster than avg
Panel avg: 131d · This submission: 53d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KNW Device Classification - Class 2, Special Controls

Product Code KNW Instrument, Biopsy
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.1075
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 Gastroenterology & Urology devices follow this clearance model.

Regulatory Peers - KNW Instrument, Biopsy

All 328
Devices cleared under the same product code (KNW) and FDA review panel - the closest regulatory comparables to K152474.
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K150625 · Apriomed AB · Jun 2015