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INTERPORE CROSS CEMENT RESTRICTOR

Page Type
Cleared 510(K)
510(k) Number
K032095
510(k) Type
Special
Applicant
Interpore Cross Intl.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2003
Days to Decision
31 days
Submission Type
Summary

INTERPORE CROSS CEMENT RESTRICTOR

Page Type
Cleared 510(K)
510(k) Number
K032095
510(k) Type
Special
Applicant
Interpore Cross Intl.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2003
Days to Decision
31 days
Submission Type
Summary