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OSTEOMED SMARTFLEX CRANIAL SPRING DISTRACTOR

Page Type
Cleared 510(K)
510(k) Number
K123885
510(k) Type
Traditional
Applicant
OSTEOMED LP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/2013
Days to Decision
167 days
Submission Type
Summary

OSTEOMED SMARTFLEX CRANIAL SPRING DISTRACTOR

Page Type
Cleared 510(K)
510(k) Number
K123885
510(k) Type
Traditional
Applicant
OSTEOMED LP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/2013
Days to Decision
167 days
Submission Type
Summary