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MOLDED CRANIAL HELMET

Page Type
Cleared 510(K)
510(k) Number
K012920
510(k) Type
Traditional
Applicant
FAIRVIEW ORTHOPEDIC LABORATORY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/28/2001
Days to Decision
90 days
Submission Type
Summary

MOLDED CRANIAL HELMET

Page Type
Cleared 510(K)
510(k) Number
K012920
510(k) Type
Traditional
Applicant
FAIRVIEW ORTHOPEDIC LABORATORY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/28/2001
Days to Decision
90 days
Submission Type
Summary