Cleared Traditional

K171592 - CrossFT™ Knotless Biocomposite Suture Anchor with Disposable Driver

K171592 is an FDA 510(k) clearance for CrossFT Knotless Biocomposite Suture An..., manufactured by Conmed Corporation. The device is a Class 2 Orthopedic device with product code MAI cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K171592 · Conmed Corporation · Orthopedic device
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Aug 2017
Decision
90d
Days
Class 2
Risk

K171592 is an FDA 510(k) clearance for the CrossFT™ Knotless Biocomposite Suture Anchor with Disposable Driver. Classified as Fastener, Fixation, Biodegradable, Soft Tissue (product code MAI), Class II - Special Controls.

Submitted by Conmed Corporation (Utica, US). The FDA issued a Cleared decision on August 29, 2017 after a review of 90 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 Conmed Corporation devices

FDA 510(k) Submission Details - K171592

510(k) Number K171592 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 31, 2017
Decision Date August 29, 2017
Days to Decision 90 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
32d faster than avg
Panel avg: 122d · This submission: 90d
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 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 K171592.
Arthrex PushLock
K173240 · Arthrex, Inc. · Jan 2018
FIXIT Threaded Anchor System
K170868 · S.B.M Sas Science For Bio Materials · Nov 2017
HEALIX ADVANCE KNOTLESS Anchor
K171114 · Medos International SARL · Nov 2017
Fixone Biocomposite Anchor
K171299 · Aju Pharm Co., Ltd. · Aug 2017
HEALIX ADVANCE Anchor with PERMATAPE Suture
K170639 · Medos International SARL · May 2017
Nanova Screw-In Suture Anchor, Nanova Push-In Suture Anchor
K163672 · Nanova Biomaterials, Inc. · May 2017