FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

FACET SCREW SYSTEM

K Number: K130863 · Decision Aug 9, 2013
Classifications
1
FEI Numbers
100
Registration Numbers
100
Same Product Code
77
Applicant Total
23
Review Days
134

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Basic Information

Device Name
FACET SCREW SYSTEM
K Number
K130863
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spinal USA
Date Received
March 28, 2013
Decision Date
August 9, 2013
Product Code
MRW
Advisory Committee
Unknown
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
MRW System, Facet Screw Spinal Device

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K Number Device Name
K132029 VAULT-C INTERVERTEBRAL BODY FUSION DEVICE
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K130445 VAULT ALIF SYSTEM
K122931 S-LOK PSS SYSTEM
K121172 REFORM PEDICLE SCREW SYSTEM
K112025 SURE LOK MINI POSTERIOR CERVICAL/UPPER THORACIC SYSTEM
K103369 VAULT ALIF SYSTEM
K092659 SPINAL USA RCS ANTERIOR LUMBAR BUTRESS PLATE SYSTEM, MODEL 22-1001-25
K092193 SPINAL USA INTERBODY CAGES
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