Zavation

Primary DI
00197157005788
Brand
Zavation
Company
Zavation LLC
Model
VCF-0810-TSK
Device description
8 Gauge 10mm Traditional Single Kyphoplasty Balloon Kit
Published
2023-12-20
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
GAANeedle, Aspiration And Injection, Disposable
HRXArthroscope
NDNCement, Bone, Vertebroplasty

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
GAANeedle, Aspiration And Injection, DisposableGeneral, Plastic Surgery1
HRXArthroscopeOrthopedic2
NDNCement, Bone, VertebroplastyOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K141419000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K141419000ZVPLASTYZavation, LLC2014-09-12NDN

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00197157005788PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00197157005788001971570057881971570057880197157005788

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
601-919-1119info@zavation.com

Regulatory Flags#

DUNS number
069472800
Device count
1
Lot or batch
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00197157117214ZAVATION SCREW1011-O-085110-S-C2026-09-21
00197157117221ZAVATION SCREW1011-O-085025-S-S2026-09-21
00197157117238ZAVATION SCREW1011-O-085030-S-S2026-09-21
00197157117245ZAVATION SCREW1011-O-085035-S-S2026-09-21
00197157117252ZAVATION SCREW1011-O-085040-S-S2026-09-21
00197157117269ZAVATION SCREW1011-O-085045-S-S2026-09-21
00197157117276ZAVATION SCREW1011-O-085050-S-S2026-09-21
00197157117283ZAVATION SCREW1011-O-085055-S-S2026-09-21
00197157117290ZAVATION SCREW1011-O-085060-S-S2026-09-21
00197157117306ZAVATION SCREW1011-O-085065-S-S2026-09-21
00197157117313ZAVATION SCREW1011-O-085070-S-S2026-09-21
00197157117320ZAVATION SCREW1011-O-085075-S-S2026-09-21
00197157117337ZAVATION SCREW1011-O-085080-S-S2026-09-21
00197157117344ZAVATION SCREW1011-O-085085-S-S2026-09-21
00197157117351ZAVATION SCREW1011-O-085090-S-S2026-09-21
00197157117368ZAVATION SCREW1011-O-085095-S-S2026-09-21
00197157117375ZAVATION SCREW1011-O-085100-S-S2026-09-21
00197157117382ZAVATION SCREW1011-O-085105-S-S2026-09-21
00197157117399ZAVATION SCREW1011-O-085110-S-S2026-09-21
00197157117405ZAVATION SCREW1011-O-085025-C-C2026-09-21

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