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INTERVERTEBRAL BODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K122872
510(k) Type
Traditional
Applicant
DIO MEDICAL CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/2013
Days to Decision
162 days
Submission Type
Summary

INTERVERTEBRAL BODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K122872
510(k) Type
Traditional
Applicant
DIO MEDICAL CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/2013
Days to Decision
162 days
Submission Type
Summary