# K900132: Acufex Sterile Cannulated Interference Screw;

- Pathway: 510(k) (Traditional)
- Applicant: Acufex Microsurgical, Inc.
- Decided: Mar 28, 1990 after 77 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
No predicates in its family tree.
11 later devices descend from it; 1 cites it directly.
0 of 12 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
- K040331: Smith and Nephew Titanium Interference Screws (2004), 10 descendants of its own
- K083619: Parcus Tintanium Interference Screw, Models: 10001-10012, 10014-10016, 10018-10020 (2009), 7 descendants of its own
- K091093: Parcus Ppek CF Interference Screw (2009), 4 descendants of its own
- K180573: Responsive Arthroscopy Interference Screw System (2018), 2 descendants of its own
- K170877: Parcus SLiK Fix Screw (2017), 1 descendant of its own

Source page: https://510kreport.com/device/K900132
Methodology: https://510kreport.com/methodology