# K895198: Hall Versipower Surgical Instrument System

- Pathway: 510(k) (Traditional)
- Applicant: Zimmer, Inc.
- Decided: Sep 15, 1989 after 35 days
- Product code: HWE (Instrument, Surgical, Orthopedic, Ac-Powered Motor And 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.
6 later devices descend from it; 3 cite it directly.
0 of 7 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
- K981269: Universal Drive System (1998), 2 descendants of its own
- K083830: Oscar Bone Resector (2009), 1 descendant of its own
- K093805: OSCAR 3 (2010), 0 descendants of its own
- K012630: Reprocessed Linvatec Arthroscopic Burs (2001), 0 descendants of its own
- K012613: Reprocssed Linvatec Shavers (2001), 0 descendants of its own

Source page: https://510kreport.com/device/K895198
Methodology: https://510kreport.com/methodology