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

LANX INTERVERTEBRAL BODY FUSION DEVICE

K Number: K073144 · Decision Jan 24, 2008
Classifications
1
FEI Numbers
418
Registration Numbers
418
Same Product Code
890
Applicant Total
13
Review Days
78

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Basic Information

Device Name
LANX INTERVERTEBRAL BODY FUSION DEVICE
K Number
K073144
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Lanx, LLC
Date Received
November 7, 2007
Decision Date
January 24, 2008
Product Code
MAX
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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

Similar 510(k) Clearances

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

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Other Clearances by Lanx, LLC

K Number Device Name
K120399 LANX SPINAL FIXATION SYSTEM
K102738 LANX FUSION SYSTEM
K103040 LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM (PCFS)
K093285 MODIFICATION TO LANX SPINAL FIXATION SYSTEM
K082774 LANX CERVICAL INTERVERTEBRAL BODY FUSION DEVICE
K071905 POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM (PCFS)
K071877 LANX SPINAL FIXATION SYSTEM
K071633 LANX DEFORMITY SYSTEM
K052384 LANX VBR SYSTEM
K043484 LANX SPINAL FIXATION SYSTEM
Search all 13 clearances from Lanx, LLC →