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

SPINEFRONTIER PEDFUSE PEDICLE SCREW SYSTEM

K Number: K133153 · Decision May 14, 2014
Classifications
1
FEI Numbers
326
Registration Numbers
326
Same Product Code
308
Applicant Total
24
Review Days
209

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Basic Information

Device Name
SPINEFRONTIER PEDFUSE PEDICLE SCREW SYSTEM
K Number
K133153
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spinefrontier, Inc.
Date Received
October 17, 2013
Decision Date
May 14, 2014
Product Code
MNH
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
MNH Orthosis, Spondylolisthesis Spinal Fixation

Similar 510(k) Clearances

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

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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
K131880 SPINEFRONTIER A-CIFT SOLOFUSE CERVICAL INTERVERTEBRAL FUSION DEVICE SYSTEM
Search all 24 clearances from Spinefrontier, Inc. →