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OSTEOMED MAXILLARY/LEFORT III DISTRACTION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031708
510(k) Type
Traditional
Applicant
OSTEOMED L.P.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/2003
Days to Decision
154 days
Submission Type
Summary

OSTEOMED MAXILLARY/LEFORT III DISTRACTION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031708
510(k) Type
Traditional
Applicant
OSTEOMED L.P.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/2003
Days to Decision
154 days
Submission Type
Summary