# K002916: Surgi-Vision Prostate Coil

- Pathway: 510(k) (Traditional)
- Applicant: Surgi-Vision, Inc.
- Decided: Nov 28, 2000 after 70 days
- Product code: MOS (Coil, Magnetic Resonance, Specialty)
- Device class: 2
- Regulation: 21 CFR 892.1000
- 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; 1 cites 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
- K011781: Intercept-Urethral Microcoil (2001), 2 descendants of its own
- K020790: Intercept Esophageal Internal MR Coil, Intercept Urethral Microcoil, and Intercept Vascular Internal MR Coil (2002), 0 descendants of its own
- K020495: Intercept Esophageal Internal MR Coil, Intercept Urethral Internal MR Coil, and Intercept Vascular Internal MR Coil (2002), 0 descendants of its own

Source page: https://510kreport.com/device/K002916
Methodology: https://510kreport.com/methodology