# K000311: Parapost Fiber White

- Pathway: 510(k) (Traditional)
- Applicant: Coltene/Whaledent, Inc.
- Decided: Mar 14, 2000 after 42 days
- Product code: ELR (Post, Root Canal)
- Device class: 1
- Regulation: 21 CFR 872.3810
- 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 lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K012354: Snowpost, Snowlight (2001), 2 descendants of its own
- K020431: Fibiocore (2002), 1 descendant of its own
- K060075: Fiber-Metal Post (2006), 0 descendants of its own

Source page: https://510kreport.com/device/K000311
Methodology: https://510kreport.com/methodology