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

SPINAL INTERVERTEBRAL BODY FIXATION ORTHOSIS

K Number: K132366 · Decision Sep 3, 2013
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
10
Review Days
35

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Basic Information

Device Name
SPINAL INTERVERTEBRAL BODY FIXATION ORTHOSIS
K Number
K132366
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Accel Spine
Date Received
July 30, 2013
Decision Date
September 3, 2013
Product Code
KWQ
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
KWQ Appliance, Fixation, Spinal Intervertebral Body

Similar 510(k) Clearances

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

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Other Clearances by Accel Spine

K Number Device Name
K140219 PICASSO II MIS SPINAL SYSTEM
K131981 CEZANNE II INTERBODY FUSION SYSTEM
K132365 SPONDYLOLISTHESIS SPINAL FIXATION, SPINAL PEDICLE FIXATION
K121567 ORACLE LUMBAR INTERVERTEBRAL BODY FUSION CAGE SYSTEM
K121568 DALI SPINAL FIXATION SYSTEM
K121078 VAN GOGH ANTERIOR CERVICAL PLATE SYSTEM
K121136 RENOIR POSTERIOR CERVIAL FIXATION SYSTEM
K120714 PICASSO MIS SPINAL FIXATION SYSTEM
K121569 MATISSE ANTERIOR CERVICAL INTERBODY FUSION CAGE SYSTEM