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BIOMET LATERAL SPACER SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122989
510(k) Type
Traditional
Applicant
Biomet Spine (Aka Ebi, LLC)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/2012
Days to Decision
28 days
Submission Type
Summary

BIOMET LATERAL SPACER SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122989
510(k) Type
Traditional
Applicant
Biomet Spine (Aka Ebi, LLC)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/2012
Days to Decision
28 days
Submission Type
Summary