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OMNIFIT BONE SCREW

Page Type
Cleared 510(K)
510(k) Number
K873251
510(k) Type
Traditional
Applicant
OSTEONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
9/18/1987
Days to Decision
32 days

OMNIFIT BONE SCREW

Page Type
Cleared 510(K)
510(k) Number
K873251
510(k) Type
Traditional
Applicant
OSTEONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
9/18/1987
Days to Decision
32 days