Last synced on 14 November 2025 at 11:06 pm

MERIDIAN CRANIAL PERFORATOR

Page Type
Cleared 510(K)
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)
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