RxG Distraction System— 510(k) K150771
Substantially EquivalentKLS Martin L.P.
FDA 510(k) clearance K150771 for RxG Distraction System, Substantially Equivalent on 2015-08-27. Applicant: KLS Martin L.P..
Clearance details
- Applicant
- KLS Martin L.P.
- Product code
- Code PBJ
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Jacksonville, FL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.