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MODIFICATION OF THE BIOPLATE ZIP CRANIOTOMY FIXATION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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