Proficient™ Posterior Cervical Spine System

Primary DI
10840642120738
Brand
Proficient™ Posterior Cervical Spine System
Company
Spine Wave, Inc.
Model
21-8437
Catalog number
21-8437
Device description
Cannulated, Extended Tab Screw, 4.2 mm X 18 mm
Published
2017-08-17
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
NKGOrthosis, Cervical Pedicle Screw Spinal Fixation

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
NKGPosterior Cervical Screw SystemOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K162639000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K162639000Proficient™ Posterior Cervical Spine SystemSpine Wave, Inc.2017-02-07NKG

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10840642120738PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized table
Source identifierGTIN-14 normalized
1084064212073810840642120738

GMDN Terms#

Term, Definition table
TermDefinition
Spinal bone screw, non-bioabsorbableA small, threaded, implantable rod with a slotted head intended to be used for internal spinal fixation by being screwed into the spine to hold a correction/stabilization device (e.g., rod, plate, tether) to bone; it is made of a material that is not chemically degraded or absorbed via natural body processes (includes implant grade metal such as surgical steel, titanium alloy, or carbon fibre). The device is available in various types, including pedicle and transfacet, and is typically used to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
203-944-9494GUDID@spinewave.com

Regulatory Flags#

DUNS number
067789763
Device count
1
Lot or batch
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
10840642132786Proficient® Posterior Cervical Spine System10-854610-85462026-10-21
10840642132793Proficient® Posterior Cervical Spine System10-854710-85472026-10-21
10840642149890Proficient® Posterior Cervical Spine System10-852910-85292026-10-21
10840642149906Proficient® Posterior Cervical Spine System10-853010-85302026-10-21
10840642151282Proficient® Posterior Cervical Spine System10-860910-86092026-10-21
10840642151305Proficient® Posterior Cervical Spine System10-861010-86102026-10-21
10840642151312Proficient® Posterior Cervical Spine System10-859610-85962026-10-21
10840642182149Spine Wave Instruments10-020510-02052026-10-21
10840642182156Spine Wave Instruments10-020610-02062026-10-21
10840642182163Spine Wave Instruments10-020710-02072026-10-21
10840642149838Proficient® Posterior Cervical Spine System10-8524.110-8524.12026-10-20
10840642149845Proficient® Posterior Cervical Spine System10-8524.210-8524.22026-10-20
10840642168709Tornado™11-58052021-10-11
10840642159615Tornado™11-58002020-04-15
10840642159622Tornado™11-58012020-04-15
10840642159639Tornado™11-58022020-04-15
10840642159646Tornado™11-58032020-04-15
10840642159653Tornado™11-58042020-04-15
10840642134797Salvo® Spine System11-671111-67112026-07-16
10840642180299Proficient® Posterior Cervical Spine System10-813110-81312026-07-13

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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