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CODERE-DURETTE ORBITAL FLOOR IMPLANT

Page Type
Cleared 510(K)
510(k) Number
K900927
510(k) Type
Traditional
Applicant
OCULO PLASTIK, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
5/15/1990
Days to Decision
77 days

CODERE-DURETTE ORBITAL FLOOR IMPLANT

Page Type
Cleared 510(K)
510(k) Number
K900927
510(k) Type
Traditional
Applicant
OCULO PLASTIK, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
5/15/1990
Days to Decision
77 days