# K920037: Osteo Compression Hip Screw

- Pathway: 510(k) (Traditional)
- Applicant: Osteo AG
- Decided: Mar 11, 1992 after 65 days
- Product code: HRC (Sterilizer, Soft-Lens, Thermal, Battery-Powered)
- Device class: 2
- Regulation: 21 CFR 886.5928
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K983508: Osteo Compression Condyle Screw System (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K920037
Methodology: https://510kreport.com/methodology