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

BIOMET FUSION SYSTEM

K Number: K141791 · Decision Oct 9, 2014
Classifications
1
FEI Numbers
253
Registration Numbers
253
Same Product Code
200
Applicant Total
19
Review Days
99

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Basic Information

Device Name
BIOMET FUSION SYSTEM
K Number
K141791
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biomet Spine
Date Received
July 2, 2014
Decision Date
October 9, 2014
Product Code
OVD
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

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Other Clearances by Biomet Spine

K Number Device Name
K152622 Alta ACDF System
K151974 Polaris Spinal System
K151064 Solitaire-C Cervical Spacer System, C-Thru Anterior Spinal System, Breckenridge Small Intervertebral Body Fusion System
K151224 Lineum OCT Spine System
K121130 POLARIS SPINAL SYSTEM-BALLISTA SPINAL RODS
K112014 ZYSTON STRAIGHT SPACER SYSTEM
K103393 POLARIS SPINAL SYSTEM
K093629 SOLITAIRE AND SOLITAIRE PEEK ANTERIOR SPINAL SYSTEM
K091067 5.5 POLARIS SPINAL SYSTEM
K082793 INTERGRO DBM
Search all 19 clearances from Biomet Spine →