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KINEMAX PLUS TIBIAL SPACERS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964951
510(k) Type
Traditional
Applicant
Howmedica Corp.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
2/24/1997
Days to Decision
76 days

KINEMAX PLUS TIBIAL SPACERS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964951
510(k) Type
Traditional
Applicant
Howmedica Corp.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
2/24/1997
Days to Decision
76 days