# K983187: Medsol Goldenberg Bone Marrow Biopsy Needle

- Pathway: 510(k) (Traditional)
- Applicant: Medsol Corp.
- Decided: Dec 10, 1998 after 90 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.
16 later devices descend from it; 2 cite it directly.
0 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K043523: Interv Brand Snarelok Bone Marrow Biopsy Needle (2005), 14 descendants of its own
- K072045: Oncontrol Bone Marrow Biopsy System (2007), 7 descendants of its own
- K081713: Vertebral Access System by Vidacare (2008), 4 descendants of its own
- K071732: Marrowminer (2007), 4 descendants of its own
- K152474: Avitus Bone Harvester (2015), 3 descendants of its own

## Indications for use
Far procuring bone marrow care biopsies from patients with hamatologic anomalities

Source page: https://510kreport.com/device/K983187
Methodology: https://510kreport.com/methodology