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BINDER 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
K093015
510(k) Type
Traditional
Applicant
BINDER BIOMEDICAL, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2010
Days to Decision
149 days
Submission Type
Summary

BINDER 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
K093015
510(k) Type
Traditional
Applicant
BINDER BIOMEDICAL, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2010
Days to Decision
149 days
Submission Type
Summary