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OSTEONICS CEMENT RESTRICTOR

Page Type
Cleared 510(K)
510(k) Number
K900462
510(k) Type
Traditional
Applicant
OSTEONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/1990
Days to Decision
34 days

OSTEONICS CEMENT RESTRICTOR

Page Type
Cleared 510(K)
510(k) Number
K900462
510(k) Type
Traditional
Applicant
OSTEONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/1990
Days to Decision
34 days