Medical Devices; Obstetrical and Gynecological Devices; Classification of the Gynecologic Laparoscopic Power Morcellation Containment System
fda-device · Food and Drug Administration · Rule · Published 2016-06-21 · Effective 2016-06-21 · 81 FR 40181
Document
Document number
2016-14627
Federal Register citation
81 FR 40181
CFR reference
21 CFR 884
Type
Rule
Action
Final order.
Category
fda-device
Sub-agency
Food and Drug Administration
Publication date
2016-06-21
Effective date
2016-06-21
HHS docket
Docket No. FDA-2016-N-1318
Abstract
The Food and Drug Administration (FDA) is classifying the gynecologic laparoscopic power morcellation containment system into class II (special controls). The special controls that will apply to the device are identified in this order and will be part of the codified language for the gynecologic laparoscopic power morcellation containment system's classification. The Agency is classifying the device into class II (special controls) in order to provide a reasonable assurance of safety and effectiveness of the device.