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

Traus SSG30 Surgical System

K Number: K232938 · Decision Sep 16, 2024
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
25
Applicant Total
18
Review Days
362

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Traus SSG30 Surgical System
K Number
K232938
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4360
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Saeshin Precision Co., Ltd.
Date Received
September 20, 2023
Decision Date
September 16, 2024
Product Code
HBC
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
HBC Motor, Drill, Electric

Similar 510(k) Clearances

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

View all

Other Clearances by Saeshin Precision Co., Ltd.

K Number Device Name
K251407 Motor Handpiece and Control Unit (SDI10)
K233153 Traus SSG10 Surgical System
K221741 TRAUS Air Dental Handpiece
K212043 TRAUS ENDO
K201292 TRAUS SIP20
K192561 TRAUS SUS20
K182892 TRAUS Dental Handpieces
K181129 STRONG Dental Handpieces
K171436 STRONG Dental Handpieces
K151171 TRAUS SUS10
Search all 18 clearances from Saeshin Precision Co., Ltd. →