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ANTERIOR ALVEOLAR RIDGE SIZER

Page Type
Cleared 510(K)
510(k) Number
K843153
510(k) Type
Traditional
Applicant
INTERPORE INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/27/1984
Days to Decision
48 days

ANTERIOR ALVEOLAR RIDGE SIZER

Page Type
Cleared 510(K)
510(k) Number
K843153
510(k) Type
Traditional
Applicant
INTERPORE INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/27/1984
Days to Decision
48 days