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

EXPEDIUM 4.5MM SPINE SYSTEM

K Number: K071495 · Decision Jun 29, 2007
Classifications
1
FEI Numbers
407
Registration Numbers
407
Same Product Code
900
Applicant Total
4
Review Days
29

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Basic Information

Device Name
EXPEDIUM 4.5MM SPINE SYSTEM
K Number
K071495
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Depuy Spine, A Johnson & Johnson Company
Date Received
May 31, 2007
Decision Date
June 29, 2007
Product Code
NKB
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
NKB Thoracolumbosacral Pedicle Screw System

Similar 510(k) Clearances

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

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Other Clearances by Depuy Spine, A Johnson & Johnson Company

K Number Device Name
K131802 EXPEDIUM, VIPER. VIPER 2 SPINE SYSTEM
K102249 EXPEDIUM SPINE SYSTEM
K071927 MODIFICATION TO VERTEBROPLASTIC RADIOPAQUE BONE CEMENT