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ORTHOCAD IQ

Page Type
Cleared 510(K)
510(k) Number
K082207
510(k) Type
Traditional
Applicant
CADENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/23/2009
Days to Decision
444 days
Submission Type
Summary

ORTHOCAD IQ

Page Type
Cleared 510(K)
510(k) Number
K082207
510(k) Type
Traditional
Applicant
CADENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/23/2009
Days to Decision
444 days
Submission Type
Summary