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

OptaBlate RF Generator, OptaBlate Probes, OptaBlate Microinfuser Infusion Device

K Number: K221074 · Decision Sep 16, 2022
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
81
Review Days
157

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Basic Information

Device Name
OptaBlate RF Generator, OptaBlate Probes, OptaBlate Microinfuser Infusion Device
K Number
K221074
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stryker Corporation
Date Received
April 12, 2022
Decision Date
September 16, 2022
Product Code
GEI
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

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