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Regulatory filing

K241517 (us_fda)

510(k) clearance for the Stryker Mako Spine application; cleared 2024.

fda 510k · cleared · decided 2024-08-27


Machine-readable surfaces

Key facts

Jurisdiction
us_fda
Filing type
fda 510k
Status
cleared
Filing number
K241517
Filing date
2024-05-29
Decision date
2024-08-27
Verification posture
verified

Applicant

Stryker

Covered models (1)

Sources (1)

  1. https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K241517

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Identity

323cbd36-995e-4d72-921a-21601749dfbc