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MODIFICATION TO THE BIOPLATE BIOCLIP CRANIOTOMY FIXATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K011380
510(k) Type
Special
Applicant
BIOPLATE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/14/2001
Days to Decision
7 days
Submission Type
Summary

MODIFICATION TO THE BIOPLATE BIOCLIP CRANIOTOMY FIXATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K011380
510(k) Type
Special
Applicant
BIOPLATE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/14/2001
Days to Decision
7 days
Submission Type
Summary