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INTERPORE IMZ CYLINDER IMPLANT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K913228
510(k) Type
Traditional
Applicant
INTERPORE INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/13/1992
Days to Decision
449 days
Submission Type
Statement

INTERPORE IMZ CYLINDER IMPLANT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K913228
510(k) Type
Traditional
Applicant
INTERPORE INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/13/1992
Days to Decision
449 days
Submission Type
Statement