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

DEPUY SPINE LATERAL SYSTEM

K Number: K090899 · Decision May 19, 2009
Classifications
1
FEI Numbers
418
Registration Numbers
418
Same Product Code
890
Applicant Total
68
Review Days
48

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Basic Information

Device Name
DEPUY SPINE LATERAL SYSTEM
K Number
K090899
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Depuy Spine, Inc.
Date Received
April 1, 2009
Decision Date
May 19, 2009
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

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Other Clearances by Depuy Spine, Inc.

K Number Device Name
K201831 CONFIDENCE Spinal Cement System
K142185 EXPEDIUM VERSE SPINE SYSTEM
K111136 EXPEDIUM SPINE SYSTEM, VIPER SYSTEM, VIPER 2 SYSTEM
K121020 VIPER SYSTEM
K110353 MOUNTAINEER OCT SPINAL SYSTEM
K110216 EXPEDIUM SYSTEM, VIPER SYSTEM
K103133 VEPER SYSTEM, EXPEDIUM SYSTEM
K101993 VIPER SYSTEM, EXPEDIUM SYSTEM
K103100 MOUNTAINEER OCT SPINAL SYSTEM
K101762 VIPER F2 FACET FIXATION SYSTEM
Search all 68 clearances from Depuy Spine, Inc. →