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

NEX-LINK SPINAL FIXATION SYSTEM VARIABLE CROSSLINK, MODEL 721-XX

K Number: K052247 · Decision Sep 14, 2005
Classifications
1
FEI Numbers
330
Registration Numbers
330
Same Product Code
429
Applicant Total
13
Review Days
27

Basic Information

Device Name
NEX-LINK SPINAL FIXATION SYSTEM VARIABLE CROSSLINK, MODEL 721-XX
K Number
K052247
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3050
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ABBOTT SPINE, INC.
Date Received
August 18, 2005
Decision Date
September 14, 2005
Product Code
KWP
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
KWP Appliance, Fixation, Spinal Interlaminal

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