FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

BIOMET MICROFIXATION MANDIBULAR FRACTURE/ RECONSTRUCTION DEVICES AND PREBENT PLATES SYSTEM

K Number: K113512 · Decision Jun 29, 2012
Classifications
1
FEI Numbers
106
Registration Numbers
106
Same Product Code
291
Applicant Total
25
Review Days
214

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
BIOMET MICROFIXATION MANDIBULAR FRACTURE/ RECONSTRUCTION DEVICES AND PREBENT PLATES SYSTEM
K Number
K113512
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
872.4760
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biomet Microfixation
Date Received
November 28, 2011
Decision Date
June 29, 2012
Product Code
JEY
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JEY Plate, Bone

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JEY), ordered by most recent decision date.

View all

Other Clearances by Biomet Microfixation

K Number Device Name
K261002 Pectus Blu System
K241709 Pectus Blu Support Bar System
K223199 2.1 x 255mm Drill, 22mm Stop
K212782 SternaLock Sternal Closure System
K212608 RibFix Blu Thoracic Fixation System
K213712 Pectus Support Bar System
K213208 Twist Drills
K202969 Biomet Microfixation OmniMax MMF System
K190576 WalterLorenz Surgical Assist Arm Scope Holder
K162974 Biomet Microfixation RibFix Blu Thoracic Fixation System
Search all 25 clearances from Biomet Microfixation →