MR-III— 510(k) K002261
Substantially EquivalentSmith & Nephew, Inc.
FDA 510(k) clearance K002261 for MR-III, Substantially Equivalent on 2000-10-23. Applicant: Smith & Nephew, Inc.. Device class: 2.
Clearance details
- Applicant
- Smith & Nephew, Inc.
- Product code
- Code GAS
- Device class
- Class 2
- Regulation
- 21 CFR 878.5000
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Andover, MA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.