ROSSITER SINUS STENT— 510(k) K951803
Substantially EquivalentSmith & Nephew Richards, Inc.
FDA 510(k) clearance K951803 for ROSSITER SINUS STENT, Substantially Equivalent on 1995-05-11. Applicant: Smith & Nephew Richards, Inc.. Device class: 1.
Clearance details
- Applicant
- Smith & Nephew Richards, Inc.
- Product code
- Code KAM
- Device class
- Class 1
- Regulation
- 21 CFR 878.4800
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bartlett, TN, US
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