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ZIMMER PATIENT SPECIFIC INSTRUMENTS SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K121640
510(k) Type
Traditional
Applicant
MATERIALISE N.V.
Country
Belgium
FDA Decision
Substantially Equivalent
Decision Date
12/5/2012
Days to Decision
184 days
Submission Type
Summary

ZIMMER PATIENT SPECIFIC INSTRUMENTS SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K121640
510(k) Type
Traditional
Applicant
MATERIALISE N.V.
Country
Belgium
FDA Decision
Substantially Equivalent
Decision Date
12/5/2012
Days to Decision
184 days
Submission Type
Summary