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MODIFICATION OF THE BIOPLATE ZIP CRANIOTOMY FIXATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K020088
510(k) Type
Special
Applicant
BIOPLATE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/2002
Days to Decision
29 days
Submission Type
Summary

MODIFICATION OF THE BIOPLATE ZIP CRANIOTOMY FIXATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K020088
510(k) Type
Special
Applicant
BIOPLATE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/2002
Days to Decision
29 days
Submission Type
Summary