The following data is part of a premarket notification filed by Civco with the FDA for Etrax Needle System, Etrax Variable Angle Needle Guidance System, Virtutrax Universal Tracker.
| Device ID | K092619 |
| 510k Number | K092619 |
| Device Name: | ETRAX NEEDLE SYSTEM, ETRAX VARIABLE ANGLE NEEDLE GUIDANCE SYSTEM, VIRTUTRAX UNIVERSAL TRACKER |
| Classification | System, Imaging, Pulsed Echo, Ultrasonic |
| Applicant | CIVCO 102 FIRST ST. SOUTH Kalona, IA 52247 |
| Contact | James Leong |
| Correspondent | Mark Job REGULATORY TECHNOLOGY SERVICES, LLC 1000 Westgate Drive, Suite 510k Saint Paul, MN 55114 |
| Product Code | IYO |
| CFR Regulation Number | 892.1560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2009-08-26 |
| Decision Date | 2009-11-13 |
| Summary: | summary |