# K072788: Storz Modulith Lithotripter SLX-F2-F180

- Pathway: 510(k) (Traditional)
- Applicant: KARL STORZ Endoscopy-America, Inc.
- Decided: Dec 26, 2007 after 86 days
- Product code: LNS (Lithotriptor, Extracorporeal Shock-Wave, Urological)
- Device class: 2
- Regulation: 21 CFR 876.5990
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to P970019 (1997). 6 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K040476: Storz Modulith, Model SLX-F2, KARL STORZ Endoscopy-America, Inc. (2004) Summary page 1.
- K063504: Econolith EM1000, Medispec, Ltd. (2007) Summary page 1.

## Most influential descendants
- K201001: Modulith SLX-F2 (2021), 0 descendants of its own

## Indications for use
The Storz MODULITH® Lithotripter SLX-F2 F180 is intended for use in the noninvasive fragmentation of urinary calculi in the kidney and upper ureter.

Source page: https://510kreport.com/device/K072788
Methodology: https://510kreport.com/methodology