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

Page Type
Cleared 510(K)
510(k) Number
K082757
510(k) Type
Special
Applicant
BIOPLATE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/1/2008
Days to Decision
12 days
Submission Type
Summary

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

Page Type
Cleared 510(K)
510(k) Number
K082757
510(k) Type
Special
Applicant
BIOPLATE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/1/2008
Days to Decision
12 days
Submission Type
Summary