# K961418: Osteomed MSS

- Pathway: 510(k) (Traditional)
- Applicant: Osteomed Corp.
- Decided: Oct 25, 1996 after 196 days
- Product code: DZL (Screw, Fixation, Intraosseous)
- Device class: 2
- Regulation: 21 CFR 872.4880
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K051871: Stoma Bone Screw (2005), 1 descendant of its own
- K132212: Dental Bone Screws; Dental Bone Screws, Continuing; Screw System TX; Screw System TX Professional (2014), 0 descendants of its own

Source page: https://510kreport.com/device/K961418
Methodology: https://510kreport.com/methodology