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

POLARIS BE RODS

K Number: K071377 · Decision Aug 6, 2007
Classifications
1
FEI Numbers
321
Registration Numbers
321
Same Product Code
429
Applicant Total
19
Review Days
81

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Basic Information

Device Name
POLARIS BE RODS
K Number
K071377
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3050
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biomet Spine
Date Received
May 17, 2007
Decision Date
August 6, 2007
Product Code
KWP
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
KWP Appliance, Fixation, Spinal Interlaminal

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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
K141791 BIOMET FUSION 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
Search all 19 clearances from Biomet Spine →