SuperSTEP™

Primary DI
M963200630
Brand
SuperSTEP™
Company
METRIC MEDICAL DEVICES, INC.
Model
20063
Catalog number
20063
Device description
Product received FDA 510(k) clearance for: Hand and Foot fragment and osteotomy fixation and joint arthrodesis, fixation of proximal tibial metaphysis osteotomy and adjunctive fixation of small bone fragments (i.e. small fragments of bone that are not comminuted to the extent and preclude staple placement). These fragments may be located in long bones such as the femur, fibula or tibia in the lower extremities; the humerus, ulna or radius in the upper extremities; the clavicle and ribs; and in flat bone such as the pelvis, scapula, and sternum. Pre-sterilized, all inclusive implant procedure tray contains: 1ea Instrument containing a Nitinol SuperSTEP™ staple implant of dimensions 20 x 20 x 20mm with a 06mm vertical step with a 2.0mm x 3.0mm leg diameter leg/bridge held in the instrument with a locking pin; 1ea 20mm spaced drill guide with step alignment; 2ea 1.5mm diameter Kirchner wire with protective tips; 1 ea 3.0mm Pull Pin, 1ea 3.0mm Drill Bit (color band red), 1ea Tamp.
Published
2018-09-07
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
MR Conditional
Rx
true
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
JDRStaple, Fixation, Bone

Product Code Classifications#

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

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
M963200630PrimaryHIBCC0

GMDN Terms#

Term, Definition table
TermDefinition
Orthopaedic bone staple, non-adjustableA non-bioabsorbable, implantable device designed to be inserted into fractured bone to achieve fixation and repair; the device may also be used to attach/secure structures (e.g., ligaments/tendons) to bone, or to reduce/cease bone growth in skeletal deformities (e.g., by being implanted across epiphysial cartilage). It is typically a curved or U-shaped device made of metal alloy material, and is not adjustable after it has been applied. Guides for drilling integrated into the handle of the staple and disposable devices associated with implantation may be included.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Device Size Text, specify0

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Special Storage Condition, Specify00Staples and instruments should not be subjected to storage or shipping temperatures in excess of 76.7°C or 170°F.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
830.535.6300sales@metricmd.com

Regulatory Flags#

DUNS number
830255506
Device count
1
DM exempt
true
Kit
true
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
M9632265L30SuperScaffold™2265L32265L32018-04-25
M9632565L30Intramedullary Fixation Scaffold (IFS)2565L32565L32016-12-13
M9632565S30Intramedullary Fixation Scaffold (IFS)2565S32565S32016-09-26
M9632585L30Intramedullary Fixation Scaffold (IFS)2585L32585L32016-12-13
M9632585S20Intramedullary Fixation Scaffold (IFS)2585S22585S22016-09-26
M9632585S30Intramedullary Fixation Scaffold (IFS)2585S32585S32016-12-13
M963IFS250Intramedullary Fixation Scaffold (IFS)IFS2.5IFS2.52016-09-26
M96316TT0LINK™ External Fixator16TT16TT2024-06-07
M96320TG0LINK™ External Fixator20TG20TG2024-06-07
M96320TT0LINK™ External Fixator20TT20TT2024-06-07
M96322000200LINK™ External Fixator2-2000202-2000202024-06-07
M9634H201020LINK™ External Fixator4H2010204H2010202024-06-07
M963C200LINK™ External FixatorC-20C-202024-06-07
M963CH20100LINK™ External FixatorCH2010CH20102024-06-07
M963174010Super Staple™ Classic17401174012016-09-26
M963200830SuperSTEP™20083200832018-09-07
M963201030SuperSTEP™20103201032018-09-07
M963166010Super Staple™ Classic16601166012017-10-31
M963168010Super Staple™ Classic16801168012016-09-26
M963169010Super Staple™ Classic16901169012016-09-26

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