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TOGGLELOC XTENDER; TOGGLELOC XL; IMPLANT KIT TOGGLELOC; IMPLANT KIT TOGGLELOC BTB, EXTENDED TOGGLELOC; TOGGLELOC; BTB TO

Page Type
Cleared 510(K)
510(k) Number
K130033
510(k) Type
Traditional
Applicant
BIOMET MANUFACTURING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/2013
Days to Decision
209 days
Submission Type
Summary

TOGGLELOC XTENDER; TOGGLELOC XL; IMPLANT KIT TOGGLELOC; IMPLANT KIT TOGGLELOC BTB, EXTENDED TOGGLELOC; TOGGLELOC; BTB TO

Page Type
Cleared 510(K)
510(k) Number
K130033
510(k) Type
Traditional
Applicant
BIOMET MANUFACTURING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/2013
Days to Decision
209 days
Submission Type
Summary