Cleared Traditional

K220319 - Asnis III Cannulated Screw System

K220319 is the FDA 510(k) clearance for Asnis III Cannulated Screw System by Stryker GmbH. It is a Class 2 Orthopedic device (product code HWC) cleared through the Traditional 510(k) pathway after a 127-day FDA review.

K220319 · Stryker GmbH · Orthopedic device
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Jun 2022
Decision
127d
Days
Class 2
Risk

K220319 is an FDA 510(k) clearance for the Asnis III Cannulated Screw System, Asnis PRO Cannulated Screw System. Classified as Screw, Fixation, Bone (product code HWC), Class II - Special Controls.

Submitted by Stryker GmbH (Mahwah, US). The FDA issued a Cleared decision on June 10, 2022 after a review of 127 days - within the typical 510(k) review window.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3040 - 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. Standard predicate reliance. 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 Stryker GmbH devices

Submission Details

510(k) Number K220319 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 03, 2022
Decision Date June 10, 2022
Days to Decision 127 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
5d slower than avg
Panel avg: 122d · This submission: 127d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code HWC Screw, Fixation, Bone
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3040
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 - HWC Screw, Fixation, Bone

All 563
Devices cleared under the same product code (HWC) and FDA review panel - the closest regulatory comparables to K220319.
Arthrex Compression FT Pins
K220839 · Arthrex, Inc. · Sep 2022
CAPTIVATE® Compression Screws
K222409 · Globus Medical, Inc. · Sep 2022
Cannulated Screws
K213614 · Maxxion Medical, LLC · Aug 2022
Hand Trauma Screw System
K220723 · Skeletal Dynamics, Inc. · May 2022
ExsoMed INnate NanoTM Lag Screw System
K220892 · Exsomed Corp. · Apr 2022
Cannulated Compression Device System
K210146 · Orthopedic Designs North America, Inc. · Apr 2022