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Ackermann Intervertebral Body Fusion Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K143450
510(k) Type
Traditional
Applicant
ACKERMANN INSTRUMENTE GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
9/16/2015
Days to Decision
288 days
Submission Type
Summary

Ackermann Intervertebral Body Fusion Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K143450
510(k) Type
Traditional
Applicant
ACKERMANN INSTRUMENTE GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
9/16/2015
Days to Decision
288 days
Submission Type
Summary