# K953433: Midas Rex Telescoping System

- Pathway: 510(k) (Traditional)
- Applicant: Midas Rex Pneumatic Tools, Inc.
- Decided: Sep 15, 1995 after 56 days
- Product code: GET (Motor, Surgical Instrument, Pneumatic Powered)
- Device class: 1
- Regulation: 21 CFR 878.4820
- Recalls of this device: 2 (0 Class I)
- 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
- K962483: Midas Rex Iii Motor (1996), 1 descendant of its own
- K970965: Midas Rex Iii Motor and Attachments (Midas Iii) (1997), 0 descendants of its own

## Recalls of this device
- Sep 1, 2005 · Not classified · Z-1574-05: Potential compromise of sterile packaging for disposable dissecting tools.
- Jan 3, 2005 · Not classified · Z-0441-05: Device is missing the sub-collet component within the dissecting tool package.

Source page: https://510kreport.com/device/K953433
Methodology: https://510kreport.com/methodology