FDA.report

Fusion Nail

Primary DI
04026575175222
Brand
Fusion Nail
Company
WALDEMAR LINK GmbH & Co. KG
Model
15-0028/08
Catalog number
15-0028/08
Device description
Fusion Nail, modular
Published
2015-11-01
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Related Records

Product Codes

CodeName
JDIProsthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
KROProsthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer
LWJProsthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented
LZOProsthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

Product Code Classifications

CodeDeviceSpecialtyClass
JDIProsthesis, Hip, Semi-Constrained, Metal/Polymer, CementedOrthopedic2
KROProsthesis, Knee, Femorotibial, Constrained, Cemented, Metal/PolymerOrthopedic2
LWJProsthesis, Hip, Semi-Constrained, Metal/Polymer, UncementedOrthopedic2
LZOProsthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedOrthopedic2

Premarket Submissions

SubmissionSupplement
K151008000

Premarket Details

SubmissionSupplementDeviceApplicantDecision dateProduct code
K151008000LINK® MEGASYSTEM-C®Waldemar Link GmbH & Co. KG2015-08-26KRO

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
04026575175222PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifierGTIN-14 normalizedEAN-13
04026575175222040265751752224026575175222

GMDN Terms

TermDefinition
Arthrodesis intramedullary nail, non-distractingA rigid rod, not intended for bone distraction, dedicated to arthrodesis/joint fusion through implantation into the intramedullary canal of a long bone [e.g., femur, tibia, humerus (including fixation of the glenoid), fibula, radius, ulna] which extends beyond the joint to an adjacent bone(s), as part of traumatic repair or reconstructive procedures. It may be of fixed or variable length to allow compression (dynamic). It is intended to be fixed to the bone with screws which may be included with the nail. This is a single-use device.

Device Sizes

TypeValueUnit
Device Size Text, specify0

Regulatory Flags

DUNS number
315675488
Device count
1
DM exempt
true
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 DIBrandModelCatalogPublished
04026575175215Fusion Nail15-0028/0715-0028/072015-11-01
04026575346677Endo Model Knee Fusion Nail FK15-8429/2115-8429/212021-01-12
04026575346684Endo Model Knee Fusion Nail FK15-8429/2215-8429/222021-01-12
04026575346691Endo Model Knee Fusion Nail FK15-8429/2315-8429/232021-01-12
04026575346707Endo Model Knee Fusion Nail FK15-8430/2115-8430/212021-01-12
04026575346714Endo Model Knee Fusion Nail FK15-8430/2215-8430/222021-01-12
04026575346721Endo Model Knee Fusion Nail FK15-8430/2315-8430/232021-01-12
04026575346738Endo Model Knee Fusion Nail FK15-8431/2115-8431/212021-01-12
04026575346745Endo Model Knee Fusion Nail FK15-8431/2215-8431/222021-01-12
04026575346752Endo Model Knee Fusion Nail FK15-8431/2315-8431/232021-01-12
04026575048168General Instrument15-80352026-02-02
04026575080106MP Reconstruction System Instruments134-011/002026-02-02
04026575080175MP Reconstruction System Instruments134-031/002026-02-02
04026575080182General Instrument134-210/002026-02-02
04026575081011MP Reconstruction System - Instruments134-212/002026-02-02
04026575081042MP Reconstruction System Instruments134-041/002026-02-02
04026575081059MP Reconstruction System Instruments134-051/002026-02-02
04026575083183Endo-Model Knee System - Endo-Model EVO Knee System - LinkOptiStems151-01/012026-02-02
04026575083206Endo-Model Knee System - Endo-Model EVO Knee System - LinkOptiStems151-05/052026-02-02
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