Cannulated Compression Screw w/ Hexalobular Drive, 4.0mm x 30mm Long

Primary DI
00810054092902
Brand
Cannulated Compression Screw w/ Hexalobular Drive, 4.0mm x 30mm Long
Company
AVANTI ORTHOPAEDICS LLC
Model
CH4030
Device description
Cannulated Compression Screw w/ Hexalobular Drive, 4.0mm x 30mm Long
Published
2022-12-09
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
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
K222967000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K222967000Avanti Orthopaedics 2.2mm and 2.7mm Cannulated Screws, Avanti Orthopaedics 3.2mm and 4.0mm Cannulated ScrewsAvanti Orthopaedics, Inc.2022-11-23HWC

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00810054092902PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00810054092902008100540929028100540929020810054092902

GMDN Terms#

Term, Definition table
TermDefinition
Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterileA non-sterile assembly of implantable devices designed for the stabilization of fractured/surgically-cut bones of the limbs (long bones), their appendages (hands, feet), pelvis, craniomaxillofacial bones, and/or for limb-joint fusion. It typically consists of a set of bone fixation plates, screws, wires, and pins made of materials that cannot be chemically degraded or absorbed via natural body processes (e.g., implant grade metal, surgical steel, titanium alloy, or carbon fibre). It may also include instruments for the attachment of the implants such as screwdrivers or drills. This device is intended to be sterilized prior to use.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
610-316-7345info@avantiortho.com

Regulatory Flags#

DUNS number
043505370
Device count
1
Lot or batch
true
Manufacturing date on label
true
Sterilization required before use
true

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00810054090106Volar PEEK Plate, 5 Hole, RightVPR052020-06-18
00810054090113Volar PEEK Plate, 7 Hole, LeftVPL072020-06-18
00810054090120Volar PEEK Plate, 7 Hole, RightVPR072020-06-18
00810054090137Volar PEEK Plate, 9 Hole, LeftVPL092020-06-18
00810054090144Volar PEEK Plate, 9 Hole, RightVPR092020-06-18
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00810054090168Volar PEEK Plate, 11 Hole, RightVPR112020-06-18
00810054090175Ulnar Plate, 5 HoleULP052020-06-18
00810054090182Ulnar Plate, 7 HoleULP072020-06-18
00810054090199Straight Plate, 6 HoleSTP062020-06-18
00810054090205Straight Plate, 8 HoleSTP082020-06-18

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