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SEARCH RESULTS FOR:
seaspine
(41 results)
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Company Name
SEASPINE ORTHOPEDICS CORPORATION (41)
Brand Name
SeaSpine Spacer System - Pacifica (7)
Shoreline ASC (6)
Disc Prep (5)
SeaSpine Spacer System - Hollywood™ (4)
Cambria (2)
PLIF Allograft (2)
Posterior Disc Prep (2)
Sierra (2)
Steerable IBD (2)
Zuma-C™ (2)
Laminoplasty (1)
Lateral Retractor (1)
NewPort (1)
RAPID Graft Delivery (1)
Sierra™ (1)
Vu cPOD (1)
Zuma-C (1)
GMDN Term Name
Orthopaedic surgical distractor, internal (9)
Bone file (8)
Vertebral body prosthesis, non-sterile (7)
Spinal implant trial (5)
Bone file/rasp, manual, reusable (3)
Bone curette, reusable (1)
Bone tap, reusable (1)
Cannulated surgical drill bit, single-use (1)
General internal orthopaedic fixation system implantation kit (1)
Orthopaedic implant driver (1)
Orthopaedic implantation sleeve, reusable (1)
Orthopaedic retractor (1)
Surgical drill guide, reusable (1)
Surgical screwdriver, reusable (1)
GMDN Term Status
Active (25)
Obsolete (16)
FDA Product Code Name
ORTHOPEDIC MANUAL SURGICAL INSTRUMENT (11)
RASP (10)
Intervertebral fusion device with integrated fixation, cervical (8)
SPINAL VERTEBRAL BODY REPLACEMENT DEVICE (4)
Intervertebral fusion device with bone graft, lumbar (2)
SCREWDRIVER (2)
APPLIANCE, FIXATION, SPINAL INTERLAMINAL (1)
CURETTE (1)
CUTTER, SURGICAL (1)
Guide, surgical, instrument (1)
ORTHOSIS, SPINAL PEDICLE FIXATION (1)
RETRACTOR (1)
TAP, BONE (1)
FDA Product Code
LXH (11)
HTR (10)
OVE (8)
MQP (4)
HXX (2)
MAX (2)
FZT (1)
FZX (1)
GAD (1)
HTF (1)
HWX (1)
KWP (1)
MNI (1)
Device Packaged As Sterile
No (41)
Sterilization Prior To Use
Yes (41)
Issuing Agency
GS1 (41)
Device Size Type
7mm (41)
Device Class
Class I (28)
Class II (13)
Implantable
No (41)
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Lateral Retractor - 10889981098889
Round Dilator, 7mm
Company Name:
SEASPINE ORTHOPEDICS CORPORATION
Version or Model:
95-6804
Commercial Distribution Status:
In Commercial Distribution
Device IDs:
10889981098889 (
Primary
)
Device Sizes:
7mm
Catalog Number:
95-6804
GMDN Terms:
Orthopaedic retractor
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