SPINERX-LDM— 510(k) K031862
Substantially EquivalentSpinerx Technology
FDA 510(k) clearance K031862 for SPINERX-LDM, Substantially Equivalent on 2003-10-31. Applicant: Spinerx Technology. Device class: 2.
Clearance details
- Applicant
- Spinerx Technology
- Product code
- Code ITH
- Device class
- Class 2
- Regulation
- 21 CFR 890.5900
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Houston, TX, US
Recent devices under product code ITH
view allData sourced from openFDA. This site is unofficial and independent of the FDA.