Last synced on 18 April 2025 at 11:05 pm

GENESIS POROUS TIBIAL TRAYS & REVISION KNEE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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