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BIOMET MICROFIXATION STERNAL CLOSURE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121302
510(k) Type
Special
Applicant
BIOMET MICROFIXATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/2012
Days to Decision
141 days
Submission Type
Summary

BIOMET MICROFIXATION STERNAL CLOSURE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121302
510(k) Type
Special
Applicant
BIOMET MICROFIXATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/2012
Days to Decision
141 days
Submission Type
Summary