FDA.reportPublic FDA data

Tracker Plus Kyphoplasty System

Primary DI
08809695619861
Brand
Tracker Plus Kyphoplasty System
Company
GS Medical Co., Ltd.
Model
GCD-FD1100
Catalog number
GCD-FD1100
Published
2022-10-24
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
HRXArthroscope
NDNCement, Bone, Vertebroplasty

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HRXArthroscopeOrthopedic2
NDNCement, Bone, VertebroplastyOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K211797000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K211797000TRACKER Plus Kyphoplasty SystemGS Medical Co., Ltd.2021-10-28NDN

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
08809695619861PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
08809695619861088096956198618809695619861

GMDN Terms#

Term, Definition table
TermDefinition
Balloon kyphoplasty kitA collection of sterile surgical instruments and devices used for the reduction of a vertebral compression fractures (VCFs) caused by trauma, cancer, or osteoporosis during a minimally invasive procedure commonly known as balloon kyphoplasty. It typically consists of a bone access needle, an osteo introducer, an inflation syringe, and the inflatable bone tamp. This procedure involves the insertion of the balloon tamp into a patient's back to reduce a vertebral body fracture by compression of cancellous bone and/or movement of the endplates as the balloon is inflated, and filling the void created with orthopaedic cement/filler to stabilize the vertebra. This is a single-use device.

Sterilization Methods#

Method table
Method
Ethylene Oxide

Contacts#

Phone, Email table
PhoneEmail
+82432377393udimail@gsmedi.com

Regulatory Flags#

DUNS number
688385418
Device count
1
Lot or batch
true
Manufacturing date on label
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
08809695601903AnyPlus®GS138-5800GS138-58002026-04-21
08809974806043PYXIS 3D Titanium Cage SystemGS132-3210PGS132-3210P2025-10-14
08809974806050PYXIS 3D Titanium Cage SystemGS132-3212PGS132-3212P2025-10-14
08809974806074PYXIS 3D Titanium Cage SystemGS132-3214PGS132-3214P2025-10-14
08809974806128PYXIS 3D Titanium Cage SystemGS132-3610PGS132-3610P2025-10-14
08809974806135PYXIS 3D Titanium Cage SystemGS132-3612PGS132-3612P2025-10-14
08809974806159PYXIS 3D Titanium Cage SystemGS132-3614PGS132-3614P2025-10-14
08809974806890PYXIS 3D Titanium Cage SystemGS132-6610PGS132-6610P2025-10-14
08809974806906PYXIS 3D Titanium Cage SystemGS132-6612PGS132-6612P2025-10-14
08809974806920PYXIS 3D Titanium Cage SystemGS132-6614PGS132-6614P2025-10-14
08800322752043AnyPlus®GS136-3500GS136-35002026-01-28
08800322752067QUASAR Standalone ACIF SystemGS136-9661GS136-96612026-01-28
08800322752074QUASAR Standalone ACIF SystemGS136-9662GS136-96622026-01-28
08800322752081QUASAR Standalone ACIF SystemGS136-9668GS136-96682026-01-28
08800322752098AnyPlus®GS136-3311GS136-33112026-01-28
08806162109351AnyPlus®GS136-1410GS136-14102026-01-28
08806162109382AnyPlus®GS136-1800GS136-18002026-01-28
08806162109399AnyPlus®GS136-1801GS136-18012026-01-28
08809695589973PYXIS 3D Titanium Cervical Cage, CloseGS110-0981GS110-09812026-01-28
08809695601859AnyPlus®GS138-5520GS138-55202026-01-28

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
10810004821085Spinal Needle SetCLARUS MEDICAL, LLCHRX2026-06-23
10810004821146Curved Cannula SetCLARUS MEDICAL, LLCHRX2026-06-23
00810004821101Digital SpineScope EndoscopeCLARUS MEDICAL, LLCHRX2026-06-22
10810004821122Spinal Introducer SetCLARUS MEDICAL, LLCHRX2026-06-22
00846338001209IEC BiPolar Cable, DisposableELLIQUENCE, LLCHRX2026-06-03
00846338001230Bipolar CableELLIQUENCE, LLCHRX2026-06-03
00846338001247Bipolar Cable - 2 Flat ProngsELLIQUENCE, LLCHRX2026-06-03
00846338001537Bipolar Cable - 2 Flat ProngsELLIQUENCE, LLCHRX2026-06-03
00846338001582IEC Power Cord 110vELLIQUENCE, LLCHRX2026-06-03
00846338001605IEC Power Cord 220v ANZ PlugELLIQUENCE, LLCHRX2026-06-03
00846338001612IEC Power Cord 220v EuropeELLIQUENCE, LLCHRX2026-06-03
00846338001629IEC Power Cord U.K. 220vELLIQUENCE, LLCHRX2026-06-03
00846338007140BiPolar Cable, DisposableELLIQUENCE, LLCHRX2026-06-02
00846338005146Neutral PlateELLIQUENCE, LLCHRX2026-06-01
00846338005320Needle PunchELLIQUENCE, LLCHRX2026-06-01
07613327601695Connected OR HubSTRYKER CORPORATIONHRX2025-06-04
07613327601701SDC4K Information Management SystemSTRYKER CORPORATIONHRX2025-06-04
08058964726452Winch Kyphoplasty Kit 15 mmG21 SRLNDN2025-02-26
08058964726469Winch Kyphoplasty Kit 20 mmG21 SRLNDN2025-02-26
08058964726735Winch Kyphoplasty Bilateral Kit 15 mmG21 SRLNDN2025-02-26
07613327545258AutoPlex VertaPlexSTRYKER CORPORATIONNDN2024-11-21
07613327638226OmnicurveSTRYKER CORPORATIONNDN2024-09-03
07613327638226OmnicurveSTRYKER CORPORATIONHRX2024-09-03
07613327638233OmnicurveSTRYKER CORPORATIONHRX2024-09-03
07613327638233OmnicurveSTRYKER CORPORATIONNDN2024-09-03
07613327638240OmnicurveSTRYKER CORPORATIONNDN2024-09-03
07613327638240OmnicurveSTRYKER CORPORATIONHRX2024-09-03
07613327638257OmnicurveSTRYKER CORPORATIONNDN2024-09-03
07613327638257OmnicurveSTRYKER CORPORATIONHRX2024-09-03
07613327638431OmnicurveSTRYKER CORPORATIONHRX2024-09-03