K171947 is an FDA 510(k) clearance for the SOLOASSIST II. This device is classified as 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 September 21, 2018, 449 days after receiving the submission on June 29, 2017.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 876.1500. 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)..
| 510(k) Number | K171947 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 29, 2017 |
| Decision Date | September 21, 2018 |
| Days to Decision | 449 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| 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). |