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COMPREHENSIVE REVERSE SHOULDER - E1 POLYETHYLENE CLAIMS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121183
510(k) Type
Traditional
Applicant
Biomet Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/2012
Days to Decision
99 days
Submission Type
Summary

COMPREHENSIVE REVERSE SHOULDER - E1 POLYETHYLENE CLAIMS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121183
510(k) Type
Traditional
Applicant
Biomet Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/2012
Days to Decision
99 days
Submission Type
Summary