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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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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