Last synced on 14 November 2025 at 11:06 pm

MODIFICATION TO BIOPLATE BIOCLIP CRANIOTOMY FIXATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K002879
510(k) Type
Special
Applicant
BIOPLATE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/2000
Days to Decision
20 days
Submission Type
Summary

MODIFICATION TO BIOPLATE BIOCLIP CRANIOTOMY FIXATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K002879
510(k) Type
Special
Applicant
BIOPLATE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/2000
Days to Decision
20 days
Submission Type
Summary