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DYNAMIK INTERVERTEBRAL BODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K081888
510(k) Type
Traditional
Applicant
SPINEART
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
2/6/2009
Days to Decision
219 days
Submission Type
Summary

DYNAMIK INTERVERTEBRAL BODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K081888
510(k) Type
Traditional
Applicant
SPINEART
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
2/6/2009
Days to Decision
219 days
Submission Type
Summary