Last synced on 10 January 2025 at 11:05 pm

HYBRIDknife® flex

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232033
510(k) Type
Traditional
Applicant
Erbe Elektromedizin GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
11/29/2023
Days to Decision
145 days
Submission Type
Summary

HYBRIDknife® flex

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232033
510(k) Type
Traditional
Applicant
Erbe Elektromedizin GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
11/29/2023
Days to Decision
145 days
Submission Type
Summary