# K072848: Activascrew

- Pathway: 510(k) (Special)
- Applicant: Bioretec, Ltd.
- Decided: Nov 2, 2007 after 29 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.
3 later devices descend from it; 2 cite 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
- K081392: Bioretec Activascrew, Activascrew Cannulated and Activascrew Cannulated with Activapin (2008), 2 descendants of its own
- K261057: ActivaScrew™ Cannulated COM (2026), 0 descendants of its own
- K130716: Bioretec Activascrew Interference (2013), 0 descendants of its own

Source page: https://510kreport.com/device/K072848
Methodology: https://510kreport.com/methodology