FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

KLS Martin IPS Forearm System

K Number: K250865 · Decision Nov 14, 2025
Classifications
1
FEI Numbers
519
Registration Numbers
519
Same Product Code
1313
Applicant Total
58
Review Days
238

Basic Information

Device Name
KLS Martin IPS Forearm System
K Number
K250865
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
KLS-Martin L.P.
Date Received
March 21, 2025
Decision Date
November 14, 2025
Product Code
HRS
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
HRS Plate, Fixation, Bone

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K252573 KLS Martin Cranial Implants - MR Conditional; K944565: KLS-Martin Micro Osteosynthesis System (1.5MM); K971297: KLS Martin Centre-Drive Drill-Free Screw; K060177: KLS Martin Rigid Fixation - Sterile; K062570: Individual Patient Solutions - Ti (IPS-Ti); K072707: Individual Patient Solutions - PEEK (IPS-PEEK) ; K151382: Individual Patient Solutions - (IPS-PEEK) - STERILE
K233721 KLS Martin Drill-Free MMF Screw
K241314 KLS Martin Oral-Max Implants MR Conditional (bundled)
K241018 KLS Martin Orthopedic Implants - MR Conditional
K230211 CranioXpand
K222624 KLS Martin LINOS Wrist System
K222397 KLS Martin Level One Rib Fixation System
K210731 KLS Martin Individual Patient Solutions
Search all 58 clearances from KLS-Martin L.P. →