STIWELL MED4— 510(k) K080950
Substantially EquivalentOtto Bock, Austria GmbH
FDA 510(k) clearance K080950 for STIWELL MED4, Substantially Equivalent on 2009-04-02. Applicant: Otto Bock, Austria GmbH. Device class: 2.
Clearance details
- Applicant
- Otto Bock, Austria GmbH
- Product code
- Code IPF
- Device class
- Class 2
- Regulation
- 21 CFR 890.5850
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- St Paul, MN, US
Recent devices under product code IPF
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