Cleared Traditional

K252081 - SportLinc Syndesmosis Device (FDA 510(k) Clearance)

Mar 2026
Decision
268d
Days
Class 2
Risk

K252081 is an FDA 510(k) clearance for the SportLinc Syndesmosis Device. This device is classified as a Washer, Bolt Nut (Class II - Special Controls, product code HTN).

Submitted by Lincotek Medical (Bartlett, US). The FDA issued a Cleared decision on March 27, 2026, 268 days after receiving the submission on July 2, 2025.

This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3030.

Submission Details

510(k) Number K252081 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 02, 2025
Decision Date March 27, 2026
Days to Decision 268 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF

Device Classification

Product Code HTN - Washer, Bolt Nut
Device Class Class II - Special Controls
CFR Regulation 21 CFR 888.3030