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OmniBone™ Bone Marrow Biopsy Kit with Power Driver, OmniBone™ Bone Biopsy Kit with Power Driver

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230015
510(k) Type
Traditional
Applicant
Laurane Medical SAS
Country
France
FDA Decision
Substantially Equivalent
Decision Date
6/16/2023
Days to Decision
164 days
Submission Type
Summary

OmniBone™ Bone Marrow Biopsy Kit with Power Driver, OmniBone™ Bone Biopsy Kit with Power Driver

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230015
510(k) Type
Traditional
Applicant
Laurane Medical SAS
Country
France
FDA Decision
Substantially Equivalent
Decision Date
6/16/2023
Days to Decision
164 days
Submission Type
Summary