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

LANX CERVICAL INTERVERTEBRAL BODY FUSION SYSTEM

K Number: K103660 · Decision Feb 28, 2011
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
23
Review Days
75

Basic Information

Device Name
LANX CERVICAL INTERVERTEBRAL BODY FUSION SYSTEM
K Number
K103660
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Lanx, Inc.
Date Received
December 15, 2010
Decision Date
February 28, 2011
Product Code
ODP
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
ODP Intervertebral Fusion Device With Bone Graft, Cervical

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Other Clearances by Lanx, Inc.

K Number Device Name
K131547 LANX FUSION SYSTEM
K131156 LANX SPINAL FIXATION SYSTEM
K123767 LANX FUSION SYSTEM- SA
K121316 LANX SPINAL FIZATION SYSTEM
K122145 LANX SPINAL FIXATION SYSTEM
K121940 LANX SPINAL FIXATION SYSTEM
K113434 LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM (PCFS)
K112388 LANX CERVICAL SA
K103091 LANX SPINAL FIXATION SYSTEM
K103237 LANX SPINAL SYSTEM
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