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

AnyPlus II Spinal Fixation System

K Number: K240350 · Decision Apr 3, 2024
Classifications
1
FEI Numbers
407
Registration Numbers
407
Same Product Code
900
Applicant Total
18
Review Days
58

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Basic Information

Device Name
AnyPlus II Spinal Fixation System
K Number
K240350
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
GS Medical Co., Ltd.
Date Received
February 5, 2024
Decision Date
April 3, 2024
Product Code
NKB
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
NKB Thoracolumbosacral Pedicle Screw System

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Other Clearances by GS Medical Co., Ltd.

K Number Device Name
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K223868 PYXIS 3D Titanium Cage System
K222041 CYGNUS-C Standalone ACIF System
K221687 Pegasus-X Expandable PLIF System
K211797 TRACKER Plus Kyphoplasty System
K200592 GS Medical AnyPlus PEEK Cage System
K192335 TRACKER Kyphoplasty System
K190170 MVP Cervical Plate System
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