Cleared Traditional

K200361 - Akros Scruture Anchor LisFranc Repair Kit

K200361 is the FDA 510(k) clearance for Akros Scruture Anchor LisFranc Repair Kit by Akros Medical. It is a Class 2 Orthopedic device (product code HTN) cleared through the Traditional 510(k) pathway after a 52-day FDA review.

K200361 · Akros Medical · Orthopedic device
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Apr 2020
Decision
52d
Days
Class 2
Risk

K200361 is an FDA 510(k) clearance for the Akros Scruture Anchor LisFranc Repair Kit. Classified as Washer, Bolt Nut (product code HTN), Class II - Special Controls.

Submitted by Akros Medical (Durham, US). The FDA issued a Cleared decision on April 6, 2020 after a review of 52 days - a notably fast clearance cycle.

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: 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 Akros Medical devices

Submission Details

510(k) Number K200361 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 14, 2020
Decision Date April 06, 2020
Days to Decision 52 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
70d faster than avg
Panel avg: 122d · This submission: 52d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code HTN Washer, Bolt Nut
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 - HTN Washer, Bolt Nut

All 65
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