# K101086: Taperloc Complete

- Pathway: 510(k) (Traditional)
- Applicant: Biomet, Inc.
- Decided: Sep 3, 2010 after 137 days
- Product code: KWA (Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component))
- Device class: 3
- Regulation: 21 CFR 888.3330
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
50 later devices descend from it; 9 cite it directly.
0 of 51 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
- K103755: Taperloc Complete, Size 5 and 6 (2011), 48 descendants of its own
- K110400: Taperloc Complete Microplasty Stem (2011), 34 descendants of its own
- K121935: Taperset Hip Small Stems (2012), 20 descendants of its own
- K161184: iNSitu Total Hip System (2016), 19 descendants of its own
- K120030: Taperloc Complete Size 4MM and XR 123 (2012), 14 descendants of its own

Source page: https://510kreport.com/device/K101086
Methodology: https://510kreport.com/methodology