FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇭 Switzerland

MectaLIF 3D Metal

K Number: K251016 · Decision Jul 17, 2025
Classifications
1
FEI Numbers
418
Registration Numbers
418
Same Product Code
890
Applicant Total
165
Review Days
106

Basic Information

Device Name
MectaLIF 3D Metal
K Number
K251016
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medacta International S.A.
Date Received
April 2, 2025
Decision Date
July 17, 2025
Product Code
MAX
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MAX), ordered by most recent decision date.

View all

Other Clearances by Medacta International S.A.

K Number Device Name
K254202 MectaLIF 3D Metal Anterior
K253940 M.U.S.T. Pedicle Screw System - Extension
K253328 GMK 3D Metal Tibial Tray Extension
K250644 MSS - Monobloc stem
K251043 Mpact 3D Metal Implants Extension – DMLS Technology
K252847 NextAR Hip Platform
K242603 MyPAO SA guides
K250338 MSS - Humeral reverse liners extension
K250450 Coated hip implants
K252225 PowerKnot High Strength Sutures
Search all 165 clearances from Medacta International S.A. →