Last synced on 14 November 2025 at 11:06 pm

MODIFICATION TO BIOPLATE RIGID BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY

Page Type
Cleared 510(K)
510(k) Number
K023665
510(k) Type
Special
Applicant
BIOPLATE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/2002
Days to Decision
22 days
Submission Type
Summary

MODIFICATION TO BIOPLATE RIGID BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY

Page Type
Cleared 510(K)
510(k) Number
K023665
510(k) Type
Special
Applicant
BIOPLATE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/2002
Days to Decision
22 days
Submission Type
Summary