# K870200: Sutter Finger Joint Prosthesis

- Pathway: 510(k) (Traditional)
- Applicant: Sutter Biomedical, Inc.
- Decided: Oct 9, 1987 after 262 days
- Product code: KYJ (Prosthesis, Finger, Constrained, Polymer)
- Device class: 2
- Regulation: 21 CFR 888.3230
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 2 cite it directly.
0 of 4 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
- K013629: Finger Joint Prosthesis (2002), 1 descendant of its own
- K220142: BRM Digitalis Spacer (2023), 0 descendants of its own
- K140453: Osteotec Silicone Finger Implant (2015), 0 descendants of its own

Source page: https://510kreport.com/device/K870200
Methodology: https://510kreport.com/methodology