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

TDM Screw System

K Number: K231860 · Decision Jan 18, 2024
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
11
Review Days
209

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Basic Information

Device Name
TDM Screw System
K Number
K231860
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Tdm Co., Ltd.
Date Received
June 23, 2023
Decision Date
January 18, 2024
Product Code
HWC
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
HWC Screw, Fixation, Bone

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Other Clearances by Tdm Co., Ltd.

K Number Device Name
K241128 TDM Plate and Screw System
K230071 Femur Reconstruction Interlocking Nail System, Femur Retrograde Interlocking Nail System, Humerus Interlocking Nail System, Tibia Interlocking Nail System, Compression Hip Nail System
K240423 TDM Anterior Cervical Plate System
K232115 TDM Large Bone Plate and Screw System
K221844 TDM Lumbar Interbody Fusion Cage System
K220285 PINE Pedicle Screw System
K191057 Park's Pectus System
K190391 TDM Plate and Screw Systems
K190830 TDM Screw Systems
K171808 TDM Plate and Screw System
Search all 11 clearances from Tdm Co., Ltd. →