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MODIFIED SCREW DESIGNS FOR USE WITH THE BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY

Page Type
Cleared 510(K)
510(k) Number
K022890
510(k) Type
Special
Applicant
BIOPLATE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/2002
Days to Decision
7 days
Submission Type
Summary

MODIFIED SCREW DESIGNS FOR USE WITH THE BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY

Page Type
Cleared 510(K)
510(k) Number
K022890
510(k) Type
Special
Applicant
BIOPLATE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/2002
Days to Decision
7 days
Submission Type
Summary