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HAPSET HYDROXYLAPATITE BONE GRAFT PLASTER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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