# K170120: EndoRotor

- Pathway: 510(k) (Traditional)
- Applicant: Interscope, Inc.
- Decided: Apr 18, 2017 after 95 days
- Product code: PTE (Endoscopic Morcellator Gastroenterology)
- Device class: 2
- Regulation: 21 CFR 884.1690
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K953695 (1995). 9 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K142029: Myosure Hysteroscopic Tissue Removal System, Hologic, Inc. (2014) Summary page 4.

## Most influential descendants
- K181127: EndoRotor Console, EndoRotor Catheters, EndoRotor Specimen Trap, EndoRotor Filter Set, EndoRotor Foot Control (2019), 0 descendants of its own

## Indications for use
The EndoRotor is intended for use in endoscopic procedures by a trained gastroenterologist to resect and remove residual tissue from the peripheral margins following EMR (Endoscopic Mucosal Resection).

Source page: https://510kreport.com/device/K170120
Methodology: https://510kreport.com/methodology