FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

InZone IST Detachment System; IZDS Connecting Cable

K Number: K251832 · Decision Oct 17, 2025
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
184
Applicant Total
32
Review Days
123

Basic Information

Device Name
InZone IST Detachment System; IZDS Connecting Cable
K Number
K251832
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
882.5950
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stryker Neurovascular
Date Received
June 16, 2025
Decision Date
October 17, 2025
Product Code
HCG
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
HCG Device, Neurovascular Embolization

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