510(k) K223767 · OLO Orthopedic Stereotaxic Instrument

Ortho Guidance Precision Knee Software, Ortho Guidance Express Knee Software, Ortho Guidance Versatile Hip Software, Ortho Q Guidance System

Applicant	Stryker Leibinger GmbH & Co KG, Freiburg Im Breisgau, DE
Decision	Substantially Equivalent, Feb 13, 2023
Received	Dec 15, 2022
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K223767

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.