PMU

Containment System, Laparoscopic Power Morcellation, With Instrument Port

Product code
PMU
Device name
Containment System, Laparoscopic Power Morcellation, With Instrument Port
Device class
Class 2
21 CFR
21 CFR 884.4050
Medical specialty
Obstetrics/Gynecology
Marketing pathway
510(K)
510(k) clearances (last 3 years)
1
Summaries archived here
1 (direct download)
510(k) clearances (all years, FDA)
4 (all years; only the last 3 years are listed here)

FDA classification 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.

Definition text from the FDA device classification database (U.S. federal government work, public domain).

510(k) clearances, last 3 years (1)

Last three years. Most recent: 2025-04-15.

NumberDecision dateApplicantDevice nameSummary
K2502122025-04-15Ark SurgicalLapBox Power Tissue Containment SystemPDF

1 summaries are archived here for direct download.

Official FDA classification page: PMU
Classification and pathway per current FDA publications. Data from openFDA (CC0).