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

DEPUY PULSE CERVICAL CAGE SYSTEM

K Number: K120517 · Decision Apr 26, 2012
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
96
Review Days
65

Basic Information

Device Name
DEPUY PULSE CERVICAL CAGE SYSTEM
K Number
K120517
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medos International SARL
Date Received
February 21, 2012
Decision Date
April 26, 2012
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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