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

BIOMET MICROFIXATION NEURO PLATING SYSTEM

K Number: K121624 · Decision Oct 12, 2012
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
41
Applicant Total
25
Review Days
133

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 NEURO PLATING SYSTEM
K Number
K121624
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5320
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biomet Microfixation
Date Received
June 1, 2012
Decision Date
October 12, 2012
Product Code
GWO
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
GWO Plate, Cranioplasty, Preformed, Alterable

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GWO), 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 →