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ARTHROTEK SET SCREW

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932721
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
8/1/1994
Days to Decision
423 days
Submission Type
Summary

ARTHROTEK SET SCREW

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932721
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
8/1/1994
Days to Decision
423 days
Submission Type
Summary