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

INERTIA PEDICLE SCREW SYSTEM

K Number: K090984 · Decision Jun 30, 2009
Classifications
1
FEI Numbers
342
Registration Numbers
342
Same Product Code
302
Applicant Total
22
Review Days
84

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Basic Information

Device Name
INERTIA PEDICLE SCREW SYSTEM
K Number
K090984
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nexxt Spine, LLC
Date Received
April 7, 2009
Decision Date
June 30, 2009
Product Code
MNI
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
MNI Orthosis, Spinal Pedicle Fixation

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Other Clearances by Nexxt Spine, LLC

K Number Device Name
K231799 INERTIA® CONNEXX™ Modular Pedicle Screw System
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K202230 NEXXT MATRIXX Stand Alone ALIF System
K202192 STRUXXURE®-L and STRUXXURE®-A Plate System
K200969 NEXXT MATRIXX System
K200543 NEXXT MATRIXX Stand Alone Cervical-Turn Lock (-TL) System
K193412 NEXXT MATRIXX System
K193370 Nexxt Matrixx System
K192687 TrellOss™-L MPF
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