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ZIMMER PATIENT SPECIFIC INSTRUMENTS, ZIMMER PATIENT SPECIFIC INSTRUMENTS PLANNER, MODEL 1.1 (4.3.0.35)

Page Type
Cleared 510(K)
510(k) Number
K091263
510(k) Type
Traditional
Applicant
MATERIALISE N.V.
Country
Belgium
FDA Decision
Substantially Equivalent
Decision Date
11/19/2009
Days to Decision
203 days
Submission Type
Summary

ZIMMER PATIENT SPECIFIC INSTRUMENTS, ZIMMER PATIENT SPECIFIC INSTRUMENTS PLANNER, MODEL 1.1 (4.3.0.35)

Page Type
Cleared 510(K)
510(k) Number
K091263
510(k) Type
Traditional
Applicant
MATERIALISE N.V.
Country
Belgium
FDA Decision
Substantially Equivalent
Decision Date
11/19/2009
Days to Decision
203 days
Submission Type
Summary