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OMNIFIT TOTAL KNEE BONE AUGMENTATION WEDGES

Page Type
Cleared 510(K)
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)
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