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FASTRESPONDER STERNAL INTRAOSSEOUS DEVICE

Page Type
Cleared 510(K)
510(k) Number
K130487
510(k) Type
Traditional
Applicant
PYNG MEDICAL CORP.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
6/25/2013
Days to Decision
120 days
Submission Type
Summary

FASTRESPONDER STERNAL INTRAOSSEOUS DEVICE

Page Type
Cleared 510(K)
510(k) Number
K130487
510(k) Type
Traditional
Applicant
PYNG MEDICAL CORP.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
6/25/2013
Days to Decision
120 days
Submission Type
Summary