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ENCODE PATIENT SPECIFIC ABUTMENT

Page Type
Cleared 510(K)
510(k) Number
K102209
510(k) Type
Traditional
Applicant
BIOMET 3I, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/2010
Days to Decision
120 days
Submission Type
Summary

ENCODE PATIENT SPECIFIC ABUTMENT

Page Type
Cleared 510(K)
510(k) Number
K102209
510(k) Type
Traditional
Applicant
BIOMET 3I, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/2010
Days to Decision
120 days
Submission Type
Summary