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FASTRESPONDER STERNAL INTRAOSSEOUS DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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