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POLARIS SPINAL SYSTEM - BALLISTA II PERCUTANEOUS SCREW PLACEMENT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123549
510(k) Type
Traditional
Applicant
BIOMET SPINE (AKA EBI, LLC)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2013
Days to Decision
98 days
Submission Type
Summary

POLARIS SPINAL SYSTEM - BALLISTA II PERCUTANEOUS SCREW PLACEMENT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123549
510(k) Type
Traditional
Applicant
BIOMET SPINE (AKA EBI, LLC)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2013
Days to Decision
98 days
Submission Type
Summary