KLS Martin Individual Patient Solutions (IPS) Planning System— 510(k) K182889
Substantially EquivalentKLS-Martin L.P.
FDA 510(k) clearance K182889 for KLS Martin Individual Patient Solutions (IPS) Planning System, Substantially Equivalent on 2019-07-26. Applicant: KLS-Martin L.P.. Device class: 2.
Clearance details
- Applicant
- KLS-Martin L.P.
- Product code
- Code PPT
- Device class
- Class 2
- Regulation
- 21 CFR 882.4310
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Jacksonville, FL, US
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