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ZIMMER PATIENT SPECIFIC INSTRUMENTS SYSTEM, VERSION 2.0

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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