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Procedure Code Category
CPT Codes
Procedure Code Descriptions
Code Status
LAM
63012
Laminectomy with removal of abnormal facets and/or pars inter-articularis with decompression of cauda equina and nerve roots for spondylolisthesis, lumbar (Gill type procedure)
No Change
LAM
63015
Laminectomy with exploration and/or decompression of spinal cord and/or cauda equina, without facetectomy, foraminotomy or discectomy (eg, spinal stenosis), more than 2 vertebral segments; cervical
No Change
LAM
63016
Laminectomy with exploration and/or decompression of spinal cord and/or cauda equina, without facetectomy, foraminotomy or discectomy (eg, spinal stenosis), more than 2 vertebral segments; thoracic
No Change
LAM
63017
Laminectomy with exploration and/or decompression of spinal cord and/or cauda equina, without facetectomy, foraminotomy or discectomy (eg, spinal stenosis), more than 2 vertebral segments; lumbar
No Change
LAM
63020
Laminotomy (hemilaminectomy), with decompression of nerve root(s), including partial facetectomy, foraminotomy and/or excision of herniated intervertebral disc; 1 interspace, cervical
No Change
LAM
63030
Laminotomy (hemilaminectomy), with decompression of nerve root(s), including partial facetectomy, foraminotomy and/or excision of herniated intervertebral disc; 1 interspace, lumbar
No Change
LAM
63035
Laminotomy (hemilaminectomy), with decompression of nerve root(s), including partial facetectomy, foraminotomy and/or excision of herniated intervertebral disc; each No changeitional interspace, cervical or lumbar (List separately in No changeition to code for primary procedure)
No Change
LAM
63040
Laminotomy (hemilaminectomy), with decompression of nerve root(s), including partial facetectomy, foraminotomy and/or excision of herniated intervertebral disc, reexploration, single interspace; cervical
No Change
LAM
63042
Laminotomy (hemilaminectomy), with decompression of nerve root(s), including partial facetectomy, foraminotomy and/or excision of herniated intervertebral disc, reexploration, single interspace; lumbar
No Change
LAM
63045
Laminectomy, facetectomy and foraminotomy (unilateral or bilateral with decompression of spinal cord, cauda equina and/or nerve root[s], [eg, spinal or lateral recess stenosis]), single vertebral segment; cervical
No Change
LAM
63046
Laminectomy, facetectomy and foraminotomy (unilateral or bilateral with decompression of spinal cord, cauda equina and/or nerve root[s], [eg, spinal or lateral recess stenosis]), single vertebral segment; thoracic
No Change
LAM
63047
Laminectomy, facetectomy and foraminotomy (unilateral or bilateral with decompression of spinal cord, cauda equina and/or nerve root[s], [eg, spinal or lateral recess stenosis]), single vertebral segment; lumbar
No Change
CPT CODE
PROCEDURE
PRICE
0
CT LIVER PELVIS w/ & w/o contrast,
0
0
CT UROGRAM w/ & w/o contrast
0
73700
CT LOWER EXTREMITY w/o contrast
0
73701
CT LOWER EXTREMITY w/ contrast
0
73702
CT LOWER EXTREMITY w/ & w/o contrast
0
72131
CT LUMBAR SPINE w/o contrast
0
72132
CT LUMBAR SPINE w/ contrast
0
G0297
CT LUNG SCREENING w/o contrast
0
70486
CT MAXILLOFACIAL w/o contrast
0
70490
CT NECK SOFT TISSUE w/o contrast
0
TEST ID
Test Name
CPT Code
WILMP
Hereditary Wilms Tumor Panel, Varies
81351 81405 81479 81479 (if appropriate for government payers)
ENDCP
Hereditary Endocrine Cancer Panel, Varies
81437
HPGLP
Hereditary Paraganglioma/Pheochromocytoma Panel, Varies
81437
THYRP
Hereditary Thyroid Cancer Panel, Varies
81201 81321 81406 81351 81479 81479 (if appropriate for government payers)
BAP1Z
BAP1-Tumor Predisposition Syndrome, BAP1 Full Gene Analysis, Varies
81479
CDHZ
Hereditary Diffuse Gastric Cancer Syndrome, CDH1, Full Gene Analysis, Varies
81406
LRCCZ
Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome, FH, Full Gene Analysis, Varies
81405
BHDZ
Birt-Hogg-Dube Syndrome, FLCN, Full Gene Analysis, Varies
81479
NF1Z
Neurofibromatosis Type 1, NF1, Full Gene Analysis, Varies
81408
PTNZ
PTEN Hamartoma Tumor Syndrome, PTEN Full Gene Analysis, Varies
81321
RETZZ
Multiple Endocrine Neoplasia Type 2 Syndrome, RET, Full Gene Analysis, Varies
81406
STK1Z
Peutz-Jeghers Syndrome, STK11, Full Gene Analysis, Varies
81405
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