Regulatory filing

K241517 (us_fda)

FDA 510(k) K241517 for Mako Spine. Also K242373 for Mako Shoulder.

fda 510k · cleared · decided 2024-06-01

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Revision history: /regulatory-filings/stryker-mako-fda-510k-k241517/history
Data documentation: /data
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Key facts

Jurisdiction: us_fda
Filing type: fda 510k
Status: cleared
Filing number: K241517
Filing date: 2024-01-01
Decision date: 2024-06-01
Verification posture: verified

Applicant

Covered models (1)

Mako

Sources (1)

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

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Identity

b009d8a7-b7ea-49e3-9963-0048a279956f