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NORMED BI-DIRECTIONAL/MULTIDIRECTIONAL JAW DISTRACTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021342
510(k) Type
Traditional
Applicant
OSTEOMEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/2002
Days to Decision
94 days
Submission Type
Summary

NORMED BI-DIRECTIONAL/MULTIDIRECTIONAL JAW DISTRACTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021342
510(k) Type
Traditional
Applicant
OSTEOMEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/2002
Days to Decision
94 days
Submission Type
Summary