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SYNTHECEL DURA REPLACEMENT DEVICES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K113071
510(k) Type
Traditional
Applicant
SYNTHES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/2012
Days to Decision
84 days
Submission Type
Summary

SYNTHECEL DURA REPLACEMENT DEVICES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K113071
510(k) Type
Traditional
Applicant
SYNTHES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/2012
Days to Decision
84 days
Submission Type
Summary