FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

Aster

K Number: K254182 · Decision Feb 26, 2026
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
20
Review Days
65

Basic Information

Device Name
Aster
K Number
K254182
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Osteonic Co., Ltd.
Date Received
December 23, 2025
Decision Date
February 26, 2026
Product Code
KWQ
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
KWQ Appliance, Fixation, Spinal Intervertebral Body

Similar 510(k) Clearances

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

View all

Other Clearances by Osteonic Co., Ltd.

K Number Device Name
K243469 SIGNEX
K243467 Fix2Lock (Biocomposite medial, Biocomposite lateral, Biocombi Self Punching)
K243470 Fix2Lock (PEEK Self Punching)
K230546 SIGNEX
K233659 Suture Wing
K231322 Fix2Lock(PEEK Self Punching)
K231326 Fix2Lock(Biocomposite medial, lateral, Biocombi Self Punching)
K210360 Neuro Plating System, Neuro Plating System Plates(NST304M02A and 61 Models), Neuro Plating System-Packaging unit(NSP-001 and 10 models), Neuro Plating System-Sterile Kit(TCN-011 and 69 models), Neuro Plating System-Screws(N15A03 and 11 models)
K211992 Ortho MI System
K210122 Sterile Bioabsorbable bone screw (Bioabsorbable ACL screw)
Search all 20 clearances from Osteonic Co., Ltd. →