# K926547: Mednext 1000 Bone Dissecting System

- Pathway: 510(k) (Traditional)
- Applicant: Mednext, Inc.
- Decided: Jul 22, 1993 after 203 days
- Product code: HSZ (Instrument, Surgical, Orthopedic, Pneumatic Powered & Accessory/Attachment)
- Device class: 1
- Regulation: 21 CFR 878.4820
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K960853: Ace System (1996), 1 descendant of its own
- K983224: XPS Drill System (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K926547
Methodology: https://510kreport.com/methodology