# K083619: Parcus Tintanium Interference Screw, Models: 10001-10012, 10014-10016, 10018-10020

- Pathway: 510(k) (Traditional)
- Applicant: Parcus Medical, LLC
- Decided: Mar 6, 2009 after 88 days
- Product code: HWC (Screw, Fixation, Bone)
- 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
Longest line of descent: 4 generations back to K915424 (1993). 14 ancestors in all.
7 later devices descend from it; 3 cite it directly.
0 of 22 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K062466: Arthrex Interference Screw, Arthrex, Inc. (2006) Summary page 1.
- K032224: Biorci Screw, Smith & Nephew, Inc. (2003) Summary page 1.
- K040331: Smith and Nephew Titanium Interference Screws, Smith & Nephew, Inc. (2004) Summary page 1.

## Most influential descendants
- K091093: Parcus Ppek CF Interference Screw (2009), 4 descendants of its own
- K170877: Parcus SLiK Fix Screw (2017), 1 descendant of its own
- K111471: Exoshape (TM) Interference Fixation Device Model 1100-00-XXXX (Varies by Size) (2011), 1 descendant of its own
- K203029: Auxilock Titanium Interference Screw (2021), 0 descendants of its own
- K202662: Parcus Titanium Interference Screws (2021), 0 descendants of its own

## Indications for use
The Parcus Titanium Interference Screw is indicated for use in the fixation of ligaments and tendons in patients requiring ligament or tendon repair.

Source page: https://510kreport.com/device/K083619
Methodology: https://510kreport.com/methodology