# K924810: Sim/Plant

- Pathway: 510(k) (Traditional)
- Applicant: Columbia Scientific, Inc.
- Decided: Jan 15, 1993 after 112 days
- Product code: JAK (System, X-Ray, Tomography, Computed)
- Device class: 2
- Regulation: 21 CFR 892.1750
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
381 later devices descend from it; 2 cite it directly.
0 of 382 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
- K033849: Simplant System (2004), 379 descendants of its own
- K073449: Surgicase (2008), 143 descendants of its own
- K073468: Mimics (2008), 141 descendants of its own
- K102795: Signature Planner; Signature Guides (2011), 99 descendants of its own
- K111863: Signature Planner,Signature Guides (2012), 71 descendants of its own

Source page: https://510kreport.com/device/K924810
Methodology: https://510kreport.com/methodology