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INTERPORE HEX HEAD IMPLANT RESTORATIVE COMPONENTS

Page Type
Cleared 510(K)
510(k) Number
K912734
510(k) Type
Traditional
Applicant
INTERPORE INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/8/1992
Days to Decision
202 days
Submission Type
Summary

INTERPORE HEX HEAD IMPLANT RESTORATIVE COMPONENTS

Page Type
Cleared 510(K)
510(k) Number
K912734
510(k) Type
Traditional
Applicant
INTERPORE INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/8/1992
Days to Decision
202 days
Submission Type
Summary