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BECKER BAND CRANIAL REMOLDING ORTHOSIS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013719
510(k) Type
Traditional
Applicant
Becker Orthopedic Appliance Co.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/2002
Days to Decision
89 days
Submission Type
Summary

BECKER BAND CRANIAL REMOLDING ORTHOSIS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013719
510(k) Type
Traditional
Applicant
Becker Orthopedic Appliance Co.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/2002
Days to Decision
89 days
Submission Type
Summary