Last synced on 18 April 2025 at 11:05 pm

PROFIX PLUS TIBIAL INSERT, PROFIX PS PLUS TIBIAL INSERT, PROFIX P/S TIBIAL INSERT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963255
510(k) Type
Traditional
Applicant
SMITH & NEPHEW, INC., ORTHOPAEDIC DIV.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
1/2/1997
Days to Decision
136 days

PROFIX PLUS TIBIAL INSERT, PROFIX PS PLUS TIBIAL INSERT, PROFIX P/S TIBIAL INSERT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963255
510(k) Type
Traditional
Applicant
SMITH & NEPHEW, INC., ORTHOPAEDIC DIV.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
1/2/1997
Days to Decision
136 days