# K900003: System Ten Model 100 Surgical System

- Pathway: 510(k) (Traditional)
- Applicant: Advanced Osseous Technologies
- Decided: Mar 16, 1990 after 73 days
- Product code: JDX (Instrument, Surgical, Sonic And Accessory/Attachment)
- Device class: 2
- Regulation: 21 CFR 888.4580
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
10 later devices descend from it; 2 cite it directly.
0 of 11 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
- K961725: Oscar Orthosonics System for Cemented Arthroplasty Revision (1996), 8 descendants of its own
- K021502: Oscar, Model OE3000 (2002), 7 descendants of its own
- K031280: Ultra-Drive 3 (2003), 4 descendants of its own
- K051053: Oscar, Model OE3000DB (2005), 3 descendants of its own
- K063531: Series 3 Lotus Laparoscopic Ultrasound Surgery System (2007), 2 descendants of its own

Source page: https://510kreport.com/device/K900003
Methodology: https://510kreport.com/methodology