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INTERPORE CYLINDRICAL HEX IMPLANT, 3.3 MM DIAMETER

Page Type
Cleared 510(K)
510(k) Number
K922732
510(k) Type
Traditional
Applicant
INTERPORE INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/1994
Days to Decision
612 days
Submission Type
Summary

INTERPORE CYLINDRICAL HEX IMPLANT, 3.3 MM DIAMETER

Page Type
Cleared 510(K)
510(k) Number
K922732
510(k) Type
Traditional
Applicant
INTERPORE INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/1994
Days to Decision
612 days
Submission Type
Summary