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MODULAR HYBRID GLENOID

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060694
510(k) Type
Traditional
Applicant
Biomet Manufacturing Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/2006
Days to Decision
271 days
Submission Type
Summary

MODULAR HYBRID GLENOID

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060694
510(k) Type
Traditional
Applicant
Biomet Manufacturing Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/2006
Days to Decision
271 days
Submission Type
Summary