# K905826: Isola Slotted Connect/Angled Slotted Connector

- Pathway: 510(k) (Traditional)
- Applicant: Acromed Corp.
- Decided: Mar 21, 1991 after 80 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.
69 later devices descend from it; 2 cite it directly.
0 of 70 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
- K133746: Polaris Spinal System (2014), 67 descendants of its own
- K143248: Reform Pedicle Screw System (2014), 30 descendants of its own
- K150856: Reform Pedicle Screw System (2015), 26 descendants of its own
- K173130: Reform® Midline Cortical Screw System (2017), 21 descendants of its own
- K150896: Vitality Spinal Fixation System (2015), 19 descendants of its own

Source page: https://510kreport.com/device/K905826
Methodology: https://510kreport.com/methodology