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

KRD1 PEDICLE SCREW SYSTEM

K Number: K092420 · Decision Nov 19, 2009
Classifications
1
FEI Numbers
342
Registration Numbers
342
Same Product Code
302
Applicant Total
24
Review Days
105

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
KRD1 PEDICLE SCREW SYSTEM
K Number
K092420
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spinefrontier, Inc.
Date Received
August 6, 2009
Decision Date
November 19, 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

Similar 510(k) Clearances

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

View all

Other Clearances by Spinefrontier, Inc.

K Number Device Name
K193106 SpineFrontier Lumbar Interbody Fusion Device System
K172484 A-CIFT SoloFuse
K151198 A-CIFT SoloFuse
K142504 SpineFrontier Lumbar Interbody Fusion Device System
K150017 SpineFrontier SIJFuse Sacroiliac Joint Fusion Device System
K143377 PedFuse Pedicle Screw System
K141333 ARENA-C TIFUSE CERVICAL INTERVERTEBRAL BODY FUSION DEVICE
K142026 SPINEFRONTIER ARENA-C HA PEEK CERVICAL INTERVERTEBRAL BODY FUSION DEVICE
K141337 ARENA-C
K133153 SPINEFRONTIER PEDFUSE PEDICLE SCREW SYSTEM
Search all 24 clearances from Spinefrontier, Inc. →