The following data is part of a premarket notification filed by Life Spine with the FDA for Arx Spinal System.
Device ID | K061600 |
510k Number | K061600 |
Device Name: | ARX SPINAL SYSTEM |
Classification | Orthosis, Spinal Pedicle Fixation |
Applicant | LIFE SPINE 2400 HASSELL ROAD SUITE 370 Hoffman Estates, IL 60195 |
Contact | Erin Malloy |
Correspondent | Erin Malloy LIFE SPINE 2400 HASSELL ROAD SUITE 370 Hoffman Estates, IL 60195 |
Product Code | MNI |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-06-08 |
Decision Date | 2006-08-22 |
Summary: | summary |