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CRANIOFACIAL ANCHORS

Page Type
Cleared 510(K)
510(k) Number
K974136
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/1998
Days to Decision
88 days
Submission Type
Summary

CRANIOFACIAL ANCHORS

Page Type
Cleared 510(K)
510(k) Number
K974136
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/1998
Days to Decision
88 days
Submission Type
Summary