Cleared Traditional

K181083 - Stryker All-PEEK Knotless Anchor System

K181083 is an FDA 510(k) clearance for Stryker All-PEEK Knotless Anchor System, manufactured by Stryker. The device is a Class 2 Orthopedic device with product code MBI cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K181083 · Stryker · Orthopedic device
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Jul 2018
Decision
90d
Days
Class 2
Risk

K181083 is an FDA 510(k) clearance for the Stryker All-PEEK Knotless Anchor System. Classified as Fastener, Fixation, Nondegradable, Soft Tissue within the MBI classification (a category for soft tissue fixation fasteners and anchoring systems), Class II - Special Controls.

Submitted by Stryker (San Jose, US). The FDA issued a Cleared decision on July 23, 2018 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 888.3040 - 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.

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FDA 510(k) Submission Details - K181083

510(k) Number K181083 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 24, 2018
Decision Date July 23, 2018
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.

MBI Device Classification - Class 2, Special Controls

Product Code MBI Fastener, Fixation, Nondegradable, Soft Tissue
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 - MBI Fastener, Fixation, Nondegradable, Soft Tissue

All 569
Devices cleared under the same product code (MBI) and FDA review panel - the closest regulatory comparables to K181083.
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K173269 · Kator, LLC · May 2018
ICONIX XBraid TT with Needles, NanoTack TT Suture Anchor
K173074 · Stryker · Apr 2018