510(k) K223770

Device
Sonopet 1Q 3 7cm 1Q Large
Applicant
Stryker Corporation
510(k) number
K223770
Product code
LFL
Decision
Substantially Equivalent (SESE)
Decision date
2023-02-16
Date received
2022-12-15
Classification name
Instrument, Ultrasonic Surgical
Medical specialty
Unknown
Review panel
Unknown
Device class
U
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Thomas Flannelly
Address
1941 Stryker Way Portage MI US 49002 49002

FDA Registration Numbers

Source Documents

510(k) summary PDF

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