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OSTEOFAB PATIENT SPECIFIC FACIAL DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K133809
510(k) Type
Traditional
Applicant
OXFORD PERFORMANCE MATERIALS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/2014
Days to Decision
224 days
Submission Type
Summary

OSTEOFAB PATIENT SPECIFIC FACIAL DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K133809
510(k) Type
Traditional
Applicant
OXFORD PERFORMANCE MATERIALS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/2014
Days to Decision
224 days
Submission Type
Summary