# K091093: Parcus Ppek CF Interference Screw

- Pathway: 510(k) (Traditional)
- Applicant: Parcus Medical, LLC
- Decided: Sep 30, 2009 after 167 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: 6 generations back to K961555 (1996). 23 ancestors in all.
4 later devices descend from it; 2 cite it directly.
0 of 28 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K083619: Parcus Tintanium Interference Screw, Models: 10001-10012, 10014-10016, 10018-10020, Parcus Medical, LLC (2009) Summary page 1.
- K083226: Smith & Nephew Peek Interference Screw, Smith & Nephew Endoscopy, Inc. (2009) Summary page 1.

## Most influential descendants
- 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
- K200428: Multi-Drive Interference Screw System (2020), 0 descendants of its own
- K132783: Exoshape Duo Soft Tissue Fastener (2013), 0 descendants of its own

## Indications for use
The Parcus PEEK CF 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/K091093
Methodology: https://510kreport.com/methodology