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

Stryker iBur hubs and cutting accessories

K Number: K210377 · Decision Jun 30, 2021
Classifications
1
FEI Numbers
140
Registration Numbers
140
Same Product Code
64
Applicant Total
81
Review Days
141

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Basic Information

Device Name
Stryker iBur hubs and cutting accessories
K Number
K210377
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4310
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stryker Corporation
Date Received
February 9, 2021
Decision Date
June 30, 2021
Product Code
HBE
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
HBE Drills, Burrs, Trephines & Accessories (Simple, Powered)

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