K192898 is an FDA 510(k) clearance for the PneumoLiner, a Containment System, Laparoscopic Power Morcellation, With Instrument Port (Class II — Special Controls, product code PMU), submitted by Advanced Surgical Concepts (Bray, IE). The FDA issued a Cleared decision on February 25, 2020, 137 days after receiving the submission on October 11, 2019. This device falls under the Obstetrics & Gynecology review panel. Regulated under 21 CFR 884.4050.
| 510(k) Number | K192898 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | October 11, 2019 |
| Decision Date | February 25, 2020 |
| Days to Decision | 137 days |
| Submission Type | Traditional |
| Review Panel | Obstetrics & Gynecology (OB) |
| Summary | Summary PDF |
| Product Code | PMU — Containment System, Laparoscopic Power Morcellation, With Instrument Port |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 884.4050 |
| Definition | Use As A Multiple Instrument Port And Tissue Containment System During Minimally Invasive Gynecologic Laparoscopic Surgery To Enable The Isolation And Containment Of Tissue Considered Benign, Resected During Single-port Or Multi-site Laparoscopic Surgery During Power Morcellation And Removal. The Device Is Compatible With Bipolar Or Electromechanical Laparoscopic Power Morcellators That Are Between 15 Mm And 18 Mm In Shaft Outer Diameter And 135 Mm And 180 Mm In Shaft Working Length And Which Have An External Component That Allows For The Proper Orientation Of The Laparoscope To Perform A Contained Morcellation. |