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OSTEOMED SMARTFLEX CRANIAL SPRING DISTRACTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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