FDA.reportPublic FDA data

Mendec Spine

Primary DI
28031497000101
Brand
Mendec Spine
Company
TECRES SPA
Model
1230
Device description
Mendec Spine is an acrylic resin for the treatment of pathological fractures of the vertebral body using a vertebroplasty or kyphoplasty procedure. Mendec Spine is a medium-high viscosity acrylic resin (PMMA-based), highly radiopaque for syringe application. The device is sold disposable and sterile
Published
2015-10-06
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
false
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
NDNCement, Bone, Vertebroplasty

Product Code Classifications#

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

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K042415000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K042415000MENDEC SPINETecres S.P.A.2005-06-09NDN

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
28031497000101PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized table
Source identifierGTIN-14 normalized
2803149700010128031497000101

GMDN Terms#

Term, Definition table
TermDefinition
Orthopaedic cement, non-antimicrobialA substance designed to be used in arthroplastic and/or osteosynthetic procedures for the fixation of polymer or metallic implants to the living bone. It may also be intended for use as a filler in the case of bone pathologies (e.g., to stabilize and reinforce vertebral body structures in vertebroplasty and kyphoplasty). It is typically made from methylmethacrylate, polymethylmethacrylate (PMMA), esters of methacrylic acid or copolymers containing polymethylmethacrylate and polystyrene; it does not contain an antimicrobial agent. Disposable devices dedicated to introduction, preparation or delivery may be packaged with the cement. After application, this device cannot be reused.

Regulatory Flags#

DUNS number
435428396
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
080314970020572Mix GunASA03102024-02-12
08031497002187GUN-01GUN-012022-09-23
08031497002330RALLY All In One Cement Gun712716102022-09-23
08031497002675Cemex System ContainerASA00302022-09-23
08031497002538Kyphon VuE™ Bone CementCT01A2022-05-13
08031497002095Conflow Bone Cement1100430252021-06-09
08031497002101Conflow G Bone Cement1100430262021-06-09
08031497002118MectaCem-X LV65.01.1032021-06-09
08031497002125MectaCem-X HV65.01.1012021-06-09
08031497002149MectaCem-X LV with Gentamicin65.01.113US2021-06-09
08031497002163MectaCem-X HV with Gentamicin65.01.111US2021-06-09
28031497000019Cemex RX1200/A2015-10-08
28031497000033CEMEX ISOPLASTIC1200/I2015-10-08
28031497000057CEMEX XL1200/S2015-10-08
28031497000071CEMEX ISOPLASTIC 1/2 PACK1220/I2015-10-08
28031497000491Cemex Genta LV1400/AG US2015-10-06
28031497000507Cemex Genta HV1400/IG US2015-10-06
08031497003894InterSpace Hip Trial, 46mm ShortIHT46S2026-02-11
08031497003900InterSpace Hip Trial, 54mm ShortIHT54S2026-02-11
08031497003917InterSpace Hip Trial, 60mm ShortIHT60S2026-02-11

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08058964729767Easy Winch 13 G, 15 mmG21 SRLNDN2026-10-19
08058964729774Easy Winch 13 G, 10 mmG21 SRLNDN2026-10-19
00763000750053CD HORIZON® Fenestrated Screw Spinal SystemMEDTRONIC SOFAMOR DANEK, INC.NDN2026-10-16
00763000750251CD HORIZON® Fenestrated Screw Spinal SystemMEDTRONIC SOFAMOR DANEK, INC.NDN2026-10-16
00763000750268CD HORIZON® Fenestrated Screw Spinal SystemMEDTRONIC SOFAMOR DANEK, INC.NDN2026-10-16
00763000750275CD HORIZON® Fenestrated Screw Spinal SystemMEDTRONIC SOFAMOR DANEK, INC.NDN2026-10-16
00763000750374CD HORIZON® Fenestrated Screw Spinal SystemMEDTRONIC SOFAMOR DANEK, INC.NDN2026-10-16
00763000750404CD HORIZON® Fenestrated Screw Spinal SystemMEDTRONIC SOFAMOR DANEK, INC.NDN2026-10-16
08058964728692Winch Kyphoplasty Balloon Catheter 15G 10 mmG21 SRLNDN2026-09-30
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