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

Esophageal TTS Stent

K Number: K240522 · Decision Mar 22, 2024
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
58
Applicant Total
1
Review Days
28

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Basic Information

Device Name
Esophageal TTS Stent
K Number
K240522
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.3610
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Taewoong Medical
Date Received
February 23, 2024
Decision Date
March 22, 2024
Product Code
ESW
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
ESW Prosthesis, Esophageal

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