# K002723: Rebar Micro Catheter: Rebar-10 (1.7F), 153 CM, Dual Marker Bands; Rebar Micro Catheter: Rebar-10 (1.7F), 170 CM, Dual MA

- Pathway: 510(k) (Special)
- Applicant: Micro Therapeutics, Inc.
- Decided: Sep 28, 2000 after 28 days
- Product code: KRA (Catheter, Continuous Flush)
- Device class: 2
- Regulation: 21 CFR 870.1210
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
4 later devices descend from it; 1 cites it directly.
0 of 5 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
- K093750: Echelon Micro Catheter, Marathon Micro Catheter, Nautica Micro Catheter Ultraflow HPC Flow Directed Micro Catheter, Reba (2009), 3 descendants of its own
- K210114: Rebar Micro Catheter (2021), 1 descendant of its own
- K243534: Micro Catheter (2025), 0 descendants of its own
- K202318: Marathon Flow Directed Micro Catheter (2020), 0 descendants of its own

Source page: https://510kreport.com/device/K002723
Methodology: https://510kreport.com/methodology