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

TRANS1 AXIALIF SYSTEM

K Number: K050965 · Decision Jun 14, 2005
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
9
Review Days
57

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Basic Information

Device Name
TRANS1 AXIALIF SYSTEM
K Number
K050965
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Trans1 Incorporated
Date Received
April 18, 2005
Decision Date
June 14, 2005
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 Trans1 Incorporated

K Number Device Name
K120991 TRANS1 INTERBODY FUSION SYSTEM
K102334 TRANS1 AXIALIF PLUS
K100210 TRANS1 LATERAL INTERVERTEBRAL FUSION DEVICE, T
K092124 AXIALIF 2L, AXIALIF 2-LEVEL SYSTEM, AXIALIF APOLLO, AXIALIF II
K073643 TRANS1 AXIALIF 2-LEVEL OR II SYSTEM
K073515 TRANS1 FACET SCREW
K073514 TRANS1 AXIAL FIXATON SYSTEM
K051856 TRANS1 FACET SCREWS