neon³™ OCT spinal stabilization

Primary DI
04052536114016
Brand
neon³™ OCT spinal stabilization
Company
Ulrich GmbH & Co. KG
Model
CS 3914-50-10
Catalog number
CS 3914-50-10
Device description
Occipital screw, Ø 5.0 mm, length 10 mm, self-tapping
Published
2018-02-14
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
MR Conditional
Rx
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
KWPAPPLIANCE, FIXATION, SPINAL INTERLAMINAL
NKGOrthosis, cervical pedicle screw spinal fixation

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KWPAppliance, Fixation, Spinal InterlaminalOrthopedic2
NKGPosterior Cervical Screw SystemOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K161032000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K161032000neon3™ universal OCT spinal stabilizationUlrich GmbH & Co. KG2016-12-22NKG

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
04052536114016PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
04052536114016040525361140164052536114016

GMDN Terms#

Term, Definition table
TermDefinition
Bone-screw internal spinal fixation system, non-sterileAn assembly of non-sterile implantable devices intended to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities, also used as an adjunct to spinal fusion [e.g., for degenerative disc disease (DDD)]. Otherwise known as a pedicle screw instrumentation system, it typically consists of a combination of anchors (e.g., bolts, hooks, pedicle screws or other types), interconnection mechanisms (incorporating nuts, screws, sleeves, or bolts), longitudinal members (e.g., plates, rods, plate/rod combinations), and/or transverse connectors. Non-sterile disposable devices associated with implantation may be included.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+4907319654152safety@ulrichmedical.com
+4973196540safety@ulrichmedical.com

Regulatory Flags#

DUNS number
315494757
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
04052536052912uCentumUL 8525-232025-08-04
04052536078264uCentumCS 71382025-08-01
04052536078271uCentumCS 71402025-08-01
04052536078295uCentumCS 71442025-08-01
04052536176823N/ACS 3993-900CS 3993-9002019-05-21
04052536164417N/ACS 3995-003-000CS 3995-003-0002018-02-14
04052536164530N/ACS 3995-002-000CS 3995-002-0002018-02-14
04052536164547N/ACS 3995-001-000CS 3995-001-0002018-02-14
04052536164554N/ACS 3995-001-001CS 3995-001-0012018-02-14
04052536164615N/ACS 3994-001-004CS 3994-001-0042018-02-14
04052536164622N/ACS 3995-001-002CS 3995-001-0022018-02-14
04052536085620N/ACS 3938-03CS 3938-032016-09-22
04052536085705N/ACS 3944-02CS 3944-022016-09-22
04052536085781N/ACS 3952-01CS 3952-012018-02-14
04052536085798N/ACS 3952-02CS 3952-022018-02-14
04052536085811N/ACS 3954-01CS 3954-012018-02-14
04052536085866N/ACS 3961CS 39612016-09-22
04052536161980N/ACS 3939-01CS 3939-012016-09-22
04052536162024N/ACS 3944-03CS 3944-032016-09-22
04052536162031N/ACS 3945-01CS 3945-012016-09-22

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