510(k) K223582

Device
MectaLock TI Triple Loaded Suture Anchor
Applicant
Medacta International S.A.
510(k) number
K223582
Product code
MBI
Decision
Substantially Equivalent (SESE)
Decision date
2023-02-24
Date received
2022-12-01
Regulation
888.3040
Classification name
Fastener, Fixation, Nondegradable, Soft Tissue
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
Stefano Baj
Address
Strada Regina Castel San Pietro (Ch) CH CH-6874 CH-6874

FDA Registration Numbers

Source Documents

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

Related GUDID Devices

Primary DIBrandCompanyPublished
07630345788030MectaLock Ti Triple Loaded Suture AnchorMedacta International SA2023-02-28
07630345788023MectaLock Ti Triple Loaded Suture AnchorMedacta International SA2023-02-28
07630345788016MectaLock Ti Triple Loaded Suture AnchorMedacta International SA2023-02-28
07630345788009MectaLock Ti Triple Loaded Suture AnchorMedacta International SA2023-02-28

Other 510(k) Records For Product Code MBI

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K252635ArthroTAK Tendon Anchor KitArthroTAK, LLC2026-05-01
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K260561Arthrex FiberTak Suture AnchorArthrex, Inc.2026-03-20
K253886Grappler Suture Anchor PCFD Tether SystemParagon 28, Inc.2026-03-17
K254176SINEFIXBAAT Medical Products B.V.2026-03-16
K251750Trax EX AnchorTrax Surgical, Inc.2026-03-12
K253693Strut Suture; No-Tie ButtonRiverpoint Medical, LLC2026-03-11
K260405FiberTape ButtonArthrex, Inc.2026-03-09
K253538TeKBrace Knotless AnchorTheramicro2026-03-06
K254306Aevumed FENIX Suture AnchorAevumed, Inc.2026-03-04
K254229Arthrex Nano FiberTak Suture AnchorArthrex, Inc.2026-03-02
K253695LigaMendRiverpoint Medical, LLC2026-02-27
K253763Y-Knotless™ Flex AnchorsConmed Corporation2026-01-29