510(k) K231208

Device
Stryker Resorbable Fixation System
Applicant
Stryker Leibinger GmbH & Co KG
510(k) number
K231208
Product code
HBW
Decision
Substantially Equivalent (SESE)
Decision date
2023-08-14
Date received
2023-04-27
Regulation
882.5360
Classification name
Fastener, Plate, Cranioplasty
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Gregory Gohl
Address
Boetzinger Strasse 41 D-79111 Freiburg DE

FDA Registration Numbers

Source Documents

510(k) summary PDF

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