Last synced on 30 November 2024 at 11:09 am

Craniomaxillofacial Distraction System (CMFD)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170818
510(k) Type
Traditional
Applicant
Synthes USA Products, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/7/2017
Days to Decision
262 days
Submission Type
Summary

Craniomaxillofacial Distraction System (CMFD)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170818
510(k) Type
Traditional
Applicant
Synthes USA Products, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/7/2017
Days to Decision
262 days
Submission Type
Summary