# K120942: Parcus Twist 4 5MM Peek Suture Anchor, Parcus Twist 5.5MM Peek Suture Anchor & Parcus Triple Twist 5.5MM Peek Suture Anc

- Pathway: 510(k) (Special)
- Applicant: Parcus Medical, LLC
- Decided: Apr 20, 2012 after 22 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.
14 later devices descend from it; 6 cite it directly.
0 of 15 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
- K170327: Parcus SLiK Anchors (2017), 5 descendants of its own
- K221135: X-Twist PEEK Suture Anchor (2022), 3 descendants of its own
- K183501: Parcus Twist AP Suture Anchors (2019), 2 descendants of its own
- K243712: WasherCap™ Mini Fixation System (Model 45) (2025), 1 descendant of its own
- K212381: VersaTap, VersaLat, DueLock, VersaTi, MiniTi (2021), 1 descendant of its own

Source page: https://510kreport.com/device/K120942
Methodology: https://510kreport.com/methodology