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MERIDIAN CRANIAL PERFORATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121253
510(k) Type
Traditional
Applicant
ADEOR MEDICAL TECHNOLOGIES GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
7/17/2012
Days to Decision
83 days
Submission Type
Summary

MERIDIAN CRANIAL PERFORATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121253
510(k) Type
Traditional
Applicant
ADEOR MEDICAL TECHNOLOGIES GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
7/17/2012
Days to Decision
83 days
Submission Type
Summary