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

LANX SPINAL FIXATION SYSTEM

K Number: K131156 · Decision May 24, 2013
Classifications
1
FEI Numbers
321
Registration Numbers
321
Same Product Code
429
Applicant Total
23
Review Days
30

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Basic Information

Device Name
LANX SPINAL FIXATION SYSTEM
K Number
K131156
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3050
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Lanx, Inc.
Date Received
April 24, 2013
Decision Date
May 24, 2013
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

Similar 510(k) Clearances

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

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Other Clearances by Lanx, Inc.

K Number Device Name
K131547 LANX FUSION SYSTEM
K123767 LANX FUSION SYSTEM- SA
K121316 LANX SPINAL FIZATION SYSTEM
K122145 LANX SPINAL FIXATION SYSTEM
K121940 LANX SPINAL FIXATION SYSTEM
K113434 LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM (PCFS)
K112388 LANX CERVICAL SA
K103091 LANX SPINAL FIXATION SYSTEM
K103237 LANX SPINAL SYSTEM
K103666 LANX LATERAL
Search all 23 clearances from Lanx, Inc. →