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ZIMMER PATIENT-SPECIFIC ABUTMENT, INTERNAL HEX, TITANIUM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071439
510(k) Type
Traditional
Applicant
ZIMMER DENTAL INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/20/2007
Days to Decision
120 days
Submission Type
Summary

ZIMMER PATIENT-SPECIFIC ABUTMENT, INTERNAL HEX, TITANIUM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071439
510(k) Type
Traditional
Applicant
ZIMMER DENTAL INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/20/2007
Days to Decision
120 days
Submission Type
Summary