SMITH & NEPHEW PATELLO-FEMORAL IMPLANT— 510(k) K051086
Substantially EquivalentSmith & Nephew, Inc.
FDA 510(k) clearance K051086 for SMITH & NEPHEW PATELLO-FEMORAL IMPLANT, Substantially Equivalent on 2005-05-31. Applicant: Smith & Nephew, Inc.. Device class: 2.
Clearance details
- Applicant
- Smith & Nephew, Inc.
- Product code
- Product code KRR
- Device class
- Class 2
- Regulation
- 21 CFR 888.3540
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Location
- Memphis, TN, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.