Cleared Traditional

K200473 - SoloAsisst II, Voice Control
(FDA 510(k) Clearance)

K200473 · Aktormed GmbH · General & Plastic Surgery
Dec 2020
Decision
300d
Days
Class 2
Risk

K200473 is an FDA 510(k) clearance for the SoloAsisst II, Voice Control, a System, Surgical, Computer Controlled Instrument (Class II — Special Controls, product code NAY), submitted by Aktormed GmbH (Barbing, DE). The FDA issued a Cleared decision on December 22, 2020, 300 days after receiving the submission on February 26, 2020. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 876.1500.

Submission Details

510(k) Number K200473 FDA.gov
FDA Decision Cleared SESE
Date Received February 26, 2020
Decision Date December 22, 2020
Days to Decision 300 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code NAY — System, Surgical, Computer Controlled Instrument
Device Class Class II — Special Controls
CFR Regulation 21 CFR 876.1500
Definition If The Device Is Reusable, Validated Reprocessing Instructions And Reprocessing Validation Data For This Device Type Must Be Included In A 510(k) Submission (82 Fr 26807, Available At Https://www.gpo.gov/fdsys/pkg/fr-2017-06-09/pdf/2017-12007.pdf).

Similar Devices — NAY System, Surgical, Computer Controlled Instrument

All 161
da Vinci Force Feedback Instruments
K253986 · Intuitive Surgical, Inc. · Mar 2026
da Vinci Surgical System (IS5000)
K251739 · Intuitive Surgical, Inc. · Jan 2026
da Vinci SP Surgical System (SP1098); da Vinci E-200 Generator
K253556 · Intuitive Surgical, Inc. · Jan 2026
da Vinci SP Surgical System (SP1098)
K252675 · Intuitive Surgical, Inc. · Dec 2025
da Vinci SP Surgical System (SP1098)
K252069 · Intuitive Surgical, Inc. · Dec 2025
da Vinci SP Surgical System (SP1098)
K251426 · Intuitive Surgical, Inc. · Oct 2025