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

LDR SPINE CERVICAL INTERBODY FUSION SYSTEM

K Number: K091088 · Decision Jul 14, 2009
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
25
Review Days
90

Basic Information

Device Name
LDR SPINE CERVICAL INTERBODY FUSION SYSTEM
K Number
K091088
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ldr Spine USA
Date Received
April 15, 2009
Decision Date
July 14, 2009
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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