510(k) K252081

Device
SportLinc Syndesmosis Device
Applicant
Lincotek Medical
510(k) number
K252081
Product code
HTN
Decision
Substantially Equivalent (SESE)
Decision date
2026-03-27
Date received
2025-07-02
Regulation
888.3030
Classification name
Washer, Bolt Nut
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Troy Walters
Address
3110 Stage Post Dr. Suite 117 Bartlett TN US 38133 38133

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

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K233531OIC FLEX-FIX™ SystemOrthopaedic Implant Company2024-02-02
K232780CC-Clip® Implant SystemCc-Instruments, Inc.2023-12-18
K232755Arthrex FiberTape and TigerTape Cerclage SuturesArthrex, Inc.2023-10-06
K221485Arthrex FiberTape and TigerTape Cerclage SuturesArthrex, Inc.2022-08-22
K220947Arthrex Knotless AC Repair DevicesArthrex, Inc.2022-06-06
K220650TriMed Ripcord DeviceTriMed, Inc.2022-06-01