Regulatory filing

fda_510k (us_fda)

FDA 510(k) for Smith+Nephew CORI Surgical System. Robotic-assisted knee surgery. First system indicated for robotic-assisted revision knee surgery.

fda 510k · cleared · decided 2020-01-01

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Key facts

Jurisdiction: us_fda
Filing type: fda 510k
Status: cleared
Filing date: 2020-01-01
Decision date: 2020-01-01
Verification posture: verified

Applicant

Covered models (1)

CORI

Sources (1)

https://www.smith-nephew.com/en-us/health-care-professionals/products/orthopaedics/cori

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Identity

887b419c-85ca-4ec7-a44d-ed0aef98076f