# K073591: Microstaar Msi Injector Foam Tip System

- Pathway: 510(k) (Traditional)
- Applicant: Staar Surgical Co.
- Decided: Mar 13, 2008 after 84 days
- Product code: MSS (Folders And Injectors, Intraocular Lens (Iol))
- Device class: 1
- Regulation: 21 CFR 886.4300
- 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’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K090161: Epiphany Injection System (2009), 3 descendants of its own
- K101782: Microstaar Msi Injector System Cartridge (2010), 2 descendants of its own
- K172375: MicroSTAAR Injector System Cartridges (2017), 0 descendants of its own
- K152357: MicroSTAAR Injector System Cartridges (2015), 0 descendants of its own

## Indications for use
The MicroSTAAR TM MSI Injector Foam Tip System is a device intended to fold and insert STAAR Surgical one and three piece Collamer® lenses for surgical placement in the human eye.

Source page: https://510kreport.com/device/K073591
Methodology: https://510kreport.com/methodology