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MODIFICATION OF THE ZPLATE-ATL ANTERIOR FIXATION SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990603
510(k) Type
Special
Applicant
Danek Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/10/1999
Days to Decision
15 days
Submission Type
Summary

MODIFICATION OF THE ZPLATE-ATL ANTERIOR FIXATION SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990603
510(k) Type
Special
Applicant
Danek Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/10/1999
Days to Decision
15 days
Submission Type
Summary