RBK PATELLA FEMORAL KNEE— 510(k) K050473
Substantially EquivalentGlobal Orthopaedic Technology, USA, Inc.
FDA 510(k) clearance K050473 for RBK PATELLA FEMORAL KNEE, Substantially Equivalent on 2005-11-14. Applicant: Global Orthopaedic Technology, USA, Inc.. Device class: 2.
Clearance details
- Applicant
- Global Orthopaedic Technology, USA, Inc.
- Product code
- Code KRR
- Device class
- Class 2
- Regulation
- 21 CFR 888.3540
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Oviedo, FL, US
Recent devices under product code KRR
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