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MODIFICATION TO SCORPIO NRG KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K071991
510(k) Type
Special
Applicant
HOWMEDICA OSTEONICS CORP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/2007
Days to Decision
26 days
Submission Type
Summary

MODIFICATION TO SCORPIO NRG KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K071991
510(k) Type
Special
Applicant
HOWMEDICA OSTEONICS CORP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/2007
Days to Decision
26 days
Submission Type
Summary