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OMNIFIT TOTAL KNEE BONE AUGMENTATION WEDGES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K874635
510(k) Type
Traditional
Applicant
OSTEONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
3/10/1988
Days to Decision
121 days

OMNIFIT TOTAL KNEE BONE AUGMENTATION WEDGES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K874635
510(k) Type
Traditional
Applicant
OSTEONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
3/10/1988
Days to Decision
121 days