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ALLEN MEDULLARY CEMENT PLUGS, ZIMMER POLY PLUG INTRAMEDULLARY SYSTEM, MODEL 8011 SERIES & 1109 & 8109 SERIES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001733
510(k) Type
Traditional
Applicant
Zimmer, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/2000
Days to Decision
13 days
Submission Type
Summary

ALLEN MEDULLARY CEMENT PLUGS, ZIMMER POLY PLUG INTRAMEDULLARY SYSTEM, MODEL 8011 SERIES & 1109 & 8109 SERIES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001733
510(k) Type
Traditional
Applicant
Zimmer, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/2000
Days to Decision
13 days
Submission Type
Summary