FDA.reportPublic FDA data

HyProCure Driver

Primary DI
M621HD5FG0
Brand
HyProCure Driver
Company
Graham Medical Technologies, L.L.C.
Model
HD-5-FG
Catalog number
HD-5-FG
Device description
HyProCure Driver. Reusable instrument, for use with the HyProCure Sinus Tarsi Implant System. Indications: HyProCure is a talotarsal stabilization device used in the treatment of talotarsal dislocation and resulting sequela. The implant is designed to stabilize the talus on the tarsal mechanism to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus on the tarsal mechanism, while allowing normal talotarsal joint motion.
Published
2017-02-14
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
HWCScrew, Fixation, Bone

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HWCScrew, Fixation, BoneOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K042030000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K042030000HYPROCURE SUBTALAR IMPLANT SYSTEMGraham Medical Technologies, LLC2004-09-16HWC

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
M621HD5FG0PrimaryHIBCC0

GMDN Terms#

Term, Definition table
TermDefinition
Orthopaedic prosthesis implantation instrument, reusableA hand-held surgical instrument intended to be used during implantation of an orthopaedic prosthesis, either manually or as a computer-assisted surgery (CAS) device, to aid in the navigation/placement of the prosthesis or other instruments. It may be used for the following applications: 1) to hold/align/fix bone preparation instruments, prosthesis, or prosthesis component; 2) to provide relative position landmarks; 3) to ascertain correct spatial orientation or limb alignment; and/or 4) as an interface between prosthesis components. This is a reusable device intended to be sterilized prior to use.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
586-677-9600xx@xx.xx

Regulatory Flags#

DUNS number
828660345
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
M621CARRYINGCASE0osteo-WEDGE Opening Wedge Bone Locking System OWCarryingCase-KitCarryingCase2017-02-14
M621CP1505FG0HyProCure Sizer 05CP15-05-FGCP15-05-FG2017-02-14
M621CP1506FG0HyProCure Sizer 06CP15-06-FGCP15-06-FG2017-02-14
M621CP1507FG0HyProCure Sizer 07CP15-07-FGCP15-07-FG2017-02-14
M621CP1508FG0HyProCure Sizer 08CP15-08-FGCP15-08-FG2017-02-14
M621CP1509FG0HyProCure Sizer 09CP15-09-FGCP15-09-FG2017-02-14
M621CP1510FG0HyProCure Sizer 10CP15-10-FGCP15-10-FG2017-02-14
M621GM150010osteo-WEDGE Depth Gauge SleeveGM-150-01GM-150-012017-04-04
M621GM150020osteo-WEDGE Depth Gauge GM-150-02GM-150-022017-04-04
M621GM150030osteo-WEDGE DriverGM-150-03GM-150-032017-04-04
M621GM150040osteo-WEDGE Screw Retainer SleeveGM-150-04GM-150-042017-04-04
M621GM160010osteo-WEDGE Drill GuideGM-160-01GM-160-012017-04-04
M621GM501000osteo-WEDGE Bone Plate 00mmGM-501-00GM-501-002017-04-04
M621GM501020osteo-WEDGE Bone Plate 02mmGM-501-02GM-501-022017-04-04
M621GM501040osteo-WEDGE Bone Plate 04mmGM-501-04GM-501-042017-04-04
M621GM501060osteo-WEDGE Bone Plate 06mmGM-501-06GM-501-062017-04-04
M621GM501080osteo-WEDGE Bone Plate 08mmGM-501-08GM-501-082017-04-04
M621GM501100osteo-WEDGE Bone Plate 10mmGM-501-10GM-501-102017-04-04
M621GMDSLL0Graham Decompression Scissors, Curved Left "11-470-11-CL (14cm/5.5"")"GM-DS-LL2017-01-27
M621GMDSLR0Graham Decompression Scissors, Curved Right"11-470-11-CR (14cm/5.5"")"GM-DS-LR2017-01-27

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