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HAPSET HYDROXYLAPATITE BONE GRAFT PLASTER

Page Type
Cleared 510(K)
510(k) Number
K910432
510(k) Type
Traditional
Applicant
LIFECORE BIOMEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/1991
Days to Decision
90 days

HAPSET HYDROXYLAPATITE BONE GRAFT PLASTER

Page Type
Cleared 510(K)
510(k) Number
K910432
510(k) Type
Traditional
Applicant
LIFECORE BIOMEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/1991
Days to Decision
90 days