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OSTEOBRIDGE IDSF INTRAMEDULLARY DIAPHYSEAL SEGMENTAL DEFECT FIXATION ROD SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051965
510(k) Type
Traditional
Applicant
MERETE MEDICAL GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/2006
Days to Decision
331 days
Submission Type
Summary

OSTEOBRIDGE IDSF INTRAMEDULLARY DIAPHYSEAL SEGMENTAL DEFECT FIXATION ROD SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051965
510(k) Type
Traditional
Applicant
MERETE MEDICAL GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/2006
Days to Decision
331 days
Submission Type
Summary