Last synced on 25 April 2025 at 11:05 pm

SYNTHES VENTROFIX MIS SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031100
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/2004
Days to Decision
332 days
Submission Type
Summary

SYNTHES VENTROFIX MIS SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031100
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/2004
Days to Decision
332 days
Submission Type
Summary