RBM— 510(k) K020480
Substantially EquivalentSmith & Nephew, Inc.
FDA 510(k) clearance K020480 for RBM, Substantially Equivalent on 2002-03-12. Applicant: Smith & Nephew, Inc.. Device class: 1.
Clearance details
- Applicant
- Smith & Nephew, Inc.
- Product code
- Code KGS
- Device class
- Class 1
- Regulation
- 21 CFR 878.4930
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Mansfield, MA, US
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