# K922299: Zeppelin Motor Drill System

- Pathway: 510(k) (Traditional)
- Applicant: Von Zeppelin Chirurgische Instrumente GmbH
- Decided: Oct 13, 1992 after 151 days
- Product code: HBE (Drills, Burrs, Trephines & Accessories (Simple, Powered))
- Device class: 2
- Regulation: 21 CFR 882.4310
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
9 later devices descend from it; 3 cite it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K013091: ZMM 2000 Zeppelin Millennium Motordrill System (2002), 6 descendants of its own
- K130755: Hicut Highspeed Instrument (2014), 4 descendants of its own
- K232684: Surgify Halo (2023), 3 descendants of its own
- K250380: Surgify Halo   (54.085.SHD.H1); Surgify Halo (54.140.SHD.H1); Surgify Halo (54.070.NVG.H1); Surgify Halo (54.125.NVG.H1); Surgify Halo (54.000.SEE.H1) (2025), 2 descendants of its own
- K251433: Surgify Halo (54.085.SHD.H1); Surgify Halo (54.140.SHD.H1); Surgify Halo (54.070.NVG.H1); Surgify Halo (54.125.NVG.H1); Surgify Halo (54.000.SEE.H1); Surgify Halo (40.070.NVG.H1); Surgify Halo (40.125.NVG.H1); Surgify Halo (40.000.SEE.H1) (2025), 1 descendant of its own

Source page: https://510kreport.com/device/K922299
Methodology: https://510kreport.com/methodology