# K002059: Amt Spinal System

- Pathway: 510(k) (Traditional)
- Applicant: Micron Precision Engineering, Inc.
- Decided: Nov 13, 2000 after 130 days
- Product code: KWP (Appliance, Fixation, Spinal Interlaminal)
- Device class: 2
- Regulation: 21 CFR 888.3050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
696 later devices descend from it; 5 cite it directly.
0 of 697 devices in its family (counting itself) have a Class I recall.

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

## Most influential descendants
- K020279: Forex Corporation, Optima, Spinal System (2002), 693 descendants of its own
- K031585: U&I, Optima, Spinal System (2003), 579 descendants of its own
- K024096: Optima, Spinal System (2003), 466 descendants of its own
- K053573: GSS Pedicle Screw System (2006), 181 descendants of its own
- K033090: Icon Polyaxial Pedicle Screw System (2004), 180 descendants of its own

Source page: https://510kreport.com/device/K002059
Methodology: https://510kreport.com/methodology