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COMPRESS SEGMENTAL HUMERAL REPLACEMENT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123297
510(k) Type
Special
Applicant
BIOMET MANUFACTUTING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2012
Days to Decision
29 days
Submission Type
Summary

COMPRESS SEGMENTAL HUMERAL REPLACEMENT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123297
510(k) Type
Special
Applicant
BIOMET MANUFACTUTING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2012
Days to Decision
29 days
Submission Type
Summary