REVCON

Primary DI
00850041704043
Brand
REVCON
Company
Voom Medical Devices, Inc
Model
VKW01001
Catalog number
VKW01001
Device description
K-Wire, Ø1.4x152.4mm
Published
2023-04-05
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
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
K223392000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K223392000REVCON (TM) Screw SystemVoom Medical Devices, Inc.2023-02-28HWC

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00850041704043PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00850041704043008500417040438500417040430850041704043

GMDN Terms#

Term, Definition table
TermDefinition
Orthopaedic bone pin, non-bioabsorbableA thin, implantable rod intended to be used for the stabilization of a bone fracture or bone grafts, or for an osteotomy or arthrodesis (internal and/or external fixation). It is typically drilled into bone and may be smooth or threaded, solid or cannulated, and/or semi-flexible. Also known as a Kirschner-wire (K-wire), it may in addition be intended to assist with the introduction of a surgical instrument and/or implant; it is not intended for implantation into the intramedullary canal (i.e., not a nail). It is made of a non-bioabsorbable material (e.g., stainless steel). Some designs may have a break-off shank and/or be coated to improve long-term fixation. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Guidewire Diameter0
Guidewire Length0

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
844-372-5489info@voommedicaldevices.com

Regulatory Flags#

DUNS number
080898988
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
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00850041704005REVCONVTR01000VTR010002023-04-05
00850041704036REVCONVKW01000VKW010002023-04-05
00850041704050REVCONVEL01000VEL010002023-04-05
00850041704067REVCONVEL01001VEL010012023-04-05
00850041704074REVCONVDG01000VDG010002023-04-05
00850041704081REVCONVDB01000VDB010002023-04-05
00850041704098REVCONVDB01001VDB010012023-04-05
00850041704104REVCONVDR01000VDR010002023-04-05
00850041704111REVCONVDR01001VDR010012023-04-05
00850041704128REVCONVHA01000VHA010002023-04-05
00850041704135REVCONVHA01001VHA010012023-04-05
00850041704142REVCONRSN3020RSN30202023-04-05
00850041704159REVCONRSN3022RSN30222023-04-05
00850041704166REVCONRSN3024RSN30242023-04-05
00850041704173REVCONRSN3026RSN30262023-04-05
00850041704180REVCONRSN3028RSN30282023-04-05
00850041704197REVCONRSN3030RSN30302023-04-05
00850041704203REVCONRSN3032RSN30322023-04-05
00850041704210REVCONRSN3034RSN30342023-04-05
00850041704227REVCONRSN3036RSN30362023-04-05

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