Regulatory filing

fda_510k (us_fda)

Momentis Surgical ANOVO second-generation robotic platform FDA 510(k) clearance. First approval was De Novo authorization.

fda 510k · cleared · decided 2026-06-01

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Key facts

Jurisdiction: us_fda
Filing type: fda 510k
Status: cleared
Decision date: 2026-06-01

Covered models (1)

ANOVO

Sources (1)

https://www.surgicalroboticstechnology.com/news/momentis-surgical-receives-fda-510k-clearance-for-second-generation-anovo-robotic-platform/

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Identity

945963dc-697e-42ba-84eb-0f9e542ba3b6