Last synced on 18 April 2025 at 11:05 pm

IQL BASIC FRAGMENT PLATE SET, IQL BASIC FRAGMENT SCREW SET, IQL SMALL FRAGMENT SET, IQL MINI FRAGMENT SET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020221
510(k) Type
Traditional
Applicant
BIOMET ORTHOPEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/2/2002
Days to Decision
70 days
Submission Type
Summary

IQL BASIC FRAGMENT PLATE SET, IQL BASIC FRAGMENT SCREW SET, IQL SMALL FRAGMENT SET, IQL MINI FRAGMENT SET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020221
510(k) Type
Traditional
Applicant
BIOMET ORTHOPEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/2/2002
Days to Decision
70 days
Submission Type
Summary