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STERILE PLATE & SCREW KIT CONFIGURATIONS FOR USE WITH THE BIOPLATE TITANIUM FIXATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K022033
510(k) Type
Special
Applicant
BIOPLATE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/2002
Days to Decision
28 days
Submission Type
Summary

STERILE PLATE & SCREW KIT CONFIGURATIONS FOR USE WITH THE BIOPLATE TITANIUM FIXATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K022033
510(k) Type
Special
Applicant
BIOPLATE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/2002
Days to Decision
28 days
Submission Type
Summary