Last synced on 14 November 2025 at 11:06 pm

THE BIOPLATE MANDIBLE FIXATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K012910
510(k) Type
Traditional
Applicant
BIOPLATE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2001
Days to Decision
82 days
Submission Type
Statement

THE BIOPLATE MANDIBLE FIXATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K012910
510(k) Type
Traditional
Applicant
BIOPLATE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2001
Days to Decision
82 days
Submission Type
Statement