# K120189: Bonetrap

- Pathway: 510(k) (Traditional)
- Applicant: Berni Farns Incorporated
- Decided: Feb 22, 2012 after 30 days
- Product code: KNW (Instrument, Biopsy)
- Device class: 2
- Regulation: 21 CFR 876.1075
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Indications for use
This biopsy instrument is used for drawing of osteomnedullary substance and or for explantation of bone marrow.

Source page: https://510kreport.com/device/K120189
Methodology: https://510kreport.com/methodology