Cleared Traditional

K180101 - HEALIX ADVANCE KNOTLESS BR Anchor

K180101 is an FDA 510(k) clearance for HEALIX ADVANCE KNOTLESS BR Anchor, manufactured by Medos International SARL. The device is a Class 2 Orthopedic device with product code MAI cleared through the Traditional 510(k) pathway after a 114-day FDA review.

K180101 · Medos International SARL · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
May 2018
Decision
114d
Days
Class 2
Risk

K180101 is an FDA 510(k) clearance for the HEALIX ADVANCE KNOTLESS BR Anchor. Classified as Fastener, Fixation, Biodegradable, Soft Tissue (product code MAI), Class II - Special Controls.

Submitted by Medos International SARL (Le Locle, CH). The FDA issued a Cleared decision on May 10, 2018 after a review of 114 days - within the typical 510(k) review window.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3030 - 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 Medos International SARL devices

FDA 510(k) Submission Details - K180101

510(k) Number K180101 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 16, 2018
Decision Date May 10, 2018
Days to Decision 114 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
8d faster than avg
Panel avg: 122d · This submission: 114d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MAI Device Classification - Class 2, Special Controls

Product Code MAI Fastener, Fixation, Biodegradable, Soft Tissue
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3030
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 Consultant

Depuy Synthesmitek, A Johnson and Johnson Company
Ashley Goncalo

The regulatory consultant manages the 510(k) submission process on behalf of the applicant - coordinating technical documentation, predicate strategy and FDA communications. Identifying the consultant behind a submission is a key signal for competitive regulatory intelligence.

Regulatory Peers - MAI Fastener, Fixation, Biodegradable, Soft Tissue

All 214
Devices cleared under the same product code (MAI) and FDA review panel - the closest regulatory comparables to K180101.
Knotless SutureTak Anchors
K180594 · Arthrex, Inc. · Jun 2018
MICRORAPTOR REGENESORB Suture Anchor
K180361 · Smith and Nephew, Inc. · May 2018
Arthrex FastThread Interference Screw
K180662 · Arthrex, Inc. · May 2018
HEALIX ADVANCE Anchor with DYNACORD Suture
K173859 · Medos International SARL · Apr 2018
Arthrex Corkscrew FT
K173788 · Arthrex, Inc. · Mar 2018
Fiji Anchor
K171228 · Sportwelding GmbH · Jan 2018