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INTERPORE 200 POROUS HYDROXYAPATITE

Page Type
Cleared 510(K)
510(k) Number
K860983
510(k) Type
Traditional
Applicant
INTERPORE INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/1986
Days to Decision
67 days

INTERPORE 200 POROUS HYDROXYAPATITE

Page Type
Cleared 510(K)
510(k) Number
K860983
510(k) Type
Traditional
Applicant
INTERPORE INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/1986
Days to Decision
67 days