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

Fix2Lock (PEEK Self Punching)

K Number: K243470 · Decision Dec 3, 2024
Classifications
1
FEI Numbers
275
Registration Numbers
275
Same Product Code
593
Applicant Total
20
Review Days
25

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Basic Information

Device Name
Fix2Lock (PEEK Self Punching)
K Number
K243470
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Osteonic Co., Ltd.
Date Received
November 8, 2024
Decision Date
December 3, 2024
Product Code
MBI
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
MBI Fastener, Fixation, Nondegradable, Soft Tissue

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Other Clearances by Osteonic Co., Ltd.

K Number Device Name
K254182 Aster
K243469 SIGNEX
K243467 Fix2Lock (Biocomposite medial, Biocomposite lateral, Biocombi 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. →