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Ackermann Intervertebral Body Fusion Device

Page Type
Cleared 510(K)
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)
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