# K952167: Imz Bone Tack System

- Pathway: 510(k) (Traditional)
- Applicant: Interpore Intl.
- Decided: Nov 21, 1995 after 197 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.
24 later devices descend from it; 3 cite it directly.
0 of 25 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
- K960914: 3I Osseous Fixation System (S) (1996), 13 descendants of its own
- K011698: Straumann GBR System (2001), 12 descendants of its own
- K973180: Imtec Bone Tac (1997), 10 descendants of its own
- K050669: Jeil Bone Fixation System (2005), 8 descendants of its own
- K022790: The Autotac System Titanium Tack (2002), 6 descendants of its own

Source page: https://510kreport.com/device/K952167
Methodology: https://510kreport.com/methodology