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INTERPORE CROSS ANTERIOR CERVICAL PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K002592
510(k) Type
Traditional
Applicant
INTERPORE CROSS INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/2000
Days to Decision
46 days
Submission Type
Summary

INTERPORE CROSS ANTERIOR CERVICAL PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K002592
510(k) Type
Traditional
Applicant
INTERPORE CROSS INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/2000
Days to Decision
46 days
Submission Type
Summary