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MEDCAD ACCUSHAPE (TM) PEEK PATIENT SPECIFIC CRANIAL / CRANIOFACIAL IMPLANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110684
510(k) Type
Traditional
Applicant
VANDUZEN DBA MEDCAD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/2011
Days to Decision
105 days
Submission Type
Summary

MEDCAD ACCUSHAPE (TM) PEEK PATIENT SPECIFIC CRANIAL / CRANIOFACIAL IMPLANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110684
510(k) Type
Traditional
Applicant
VANDUZEN DBA MEDCAD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/2011
Days to Decision
105 days
Submission Type
Summary