# K222363: Aevumed PHANTOM™-LP Suture Anchors

- Pathway: 510(k) (Traditional)
- Applicant: Aevumed, Inc.
- Decided: Nov 28, 2022 after 116 days
- Product code: MBI (Fastener, Fixation, Nondegradable, Soft Tissue)
- Device class: 2
- Regulation: 21 CFR 888.3040
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 1 cites it directly.
0 of 4 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
- K260004: Aevumed PROTEKT Suture Anchor (2026), 2 descendants of its own
- K252635: ArthroTAK Tendon Anchor Kit (2026), 1 descendant of its own
- K262809: ArthroTAK Tendon Anchor Kit (2026), 0 descendants of its own

Source page: https://510kreport.com/device/K222363
Methodology: https://510kreport.com/methodology