Last synced on 12 July 2024 at 11:04 pm

RF LESION CANNULA, RF THERMOLESION CANNULA, THERMOLESION CANNULA, X-RAY CONTRAST CANNULA, CANNULA, FACET DENERATION NEED

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060397
510(k) Type
Traditional
Applicant
PAJUNK GMBH MEDIZINTECHNOLOGIE
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
8/31/2006
Days to Decision
197 days
Submission Type
Summary

RF LESION CANNULA, RF THERMOLESION CANNULA, THERMOLESION CANNULA, X-RAY CONTRAST CANNULA, CANNULA, FACET DENERATION NEED

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060397
510(k) Type
Traditional
Applicant
PAJUNK GMBH MEDIZINTECHNOLOGIE
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
8/31/2006
Days to Decision
197 days
Submission Type
Summary