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

LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM (PCFS)

K Number: K113434 · Decision Dec 19, 2011
Classifications
1
FEI Numbers
413
Registration Numbers
413
Same Product Code
873
Applicant Total
22
Review Days
28

Basic Information

Device Name
LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM (PCFS)
K Number
K113434
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
LANX, INC.
Date Received
November 21, 2011
Decision Date
December 19, 2011
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

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Other Clearances by LANX, INC.

K Number Device Name
K131547 LANX FUSION SYSTEM
K131156 LANX SPINAL FIXATION SYSTEM
K123767 LANX FUSION SYSTEM- SA
K121316 LANX SPINAL FIZATION SYSTEM
K122145 LANX SPINAL FIXATION SYSTEM
K121940 LANX SPINAL FIXATION SYSTEM
K103091 LANX SPINAL FIXATION SYSTEM
K103237 LANX SPINAL SYSTEM
K103666 LANX LATERAL
K103660 LANX CERVICAL INTERVERTEBRAL BODY FUSION SYSTEM
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