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ZIMMER PATIENT SPECIFIC INSTRUMENTS SYSTEM, VERSION 2.0

Page Type
Cleared 510(K)
510(k) Number
K093533
510(k) Type
Traditional
Applicant
MATERIALISE N.V.
Country
Belgium
FDA Decision
Substantially Equivalent
Decision Date
2/17/2010
Days to Decision
93 days
Submission Type
Summary

ZIMMER PATIENT SPECIFIC INSTRUMENTS SYSTEM, VERSION 2.0

Page Type
Cleared 510(K)
510(k) Number
K093533
510(k) Type
Traditional
Applicant
MATERIALISE N.V.
Country
Belgium
FDA Decision
Substantially Equivalent
Decision Date
2/17/2010
Days to Decision
93 days
Submission Type
Summary