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GENESIS POROUS TIBIAL TRAYS & REVISION KNEE SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K953274
510(k) Type
Traditional
Applicant
Smith & Nephew Richards, Inc.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
2/5/1996
Days to Decision
206 days

GENESIS POROUS TIBIAL TRAYS & REVISION KNEE SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K953274
510(k) Type
Traditional
Applicant
Smith & Nephew Richards, Inc.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
2/5/1996
Days to Decision
206 days