# K900510: Pertac-Hybrid

- Pathway: 510(k) (Traditional)
- Applicant: Espe GmbH (Us)
- Decided: Aug 9, 1990 after 188 days
- Product code: EBF (Material, Tooth Shade, Resin)
- Device class: 2
- Regulation: 21 CFR 872.3690
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
94 later devices descend from it; 2 cite it directly.
0 of 95 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
- K962440: Pertac II/Pertac II Aplitip (1996), 90 descendants of its own
- K974458: Compolute Aplicap (1998), 70 descendants of its own
- K020256: Unicem (2002), 63 descendants of its own
- K992645: Sinfony (1999), 59 descendants of its own
- K043043: Hermes Bond 2 (2005), 37 descendants of its own

Source page: https://510kreport.com/device/K900510
Methodology: https://510kreport.com/methodology