FDA.reportPublic FDA data

Biolign Rotoloc

Primary DI
06009708425621
Brand
Biolign Rotoloc
Company
ELITE SURGICAL SUPPLIES (PTY) LTD
Model
RLSS4216
Catalog number
RLSS4216
Device description
Roto-Loc Variable Angled Cervical Screw 4.2 x 16mm
Published
2021-07-21
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
MR Conditional
Rx
true
Single use
true

Product Codes#

Code, Name table
CodeName
KWQAppliance, Fixation, Spinal Intervertebral Body

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KWQAppliance, Fixation, Spinal Intervertebral BodyOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K200523000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K200523000Biolign® Roto-Loc Cervical Plate SystemElite Surgical Supplies (Pty), Ltd.2020-04-30KWQ

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
06009708425621PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
06009708425621060097084256216009708425621

GMDN Terms#

Term, Definition table
TermDefinition
Spinal fixation plate, non-bioabsorbableA small implantable sheet of solid material that is attached to the spine with screws for spinal immobilization and 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 typically used to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities (e.g., during anterior/posterior cervical, anterior/posterior lumbar, thoracolumbar, and occipital fixation procedures).

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Length16Millimeter

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
568359710
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
06009696221076VertefixSP5535TSP5535T2016-09-22
06009696221083VertefixSP5540TSP5540T2016-09-23
06009696221090VertefixSP5545TSP5545T2016-09-23
06009696221106VertefixSP5550TSP5550T2016-09-23
06009696221120VertefixSP6535TSP6535T2016-09-23
06009696221137VertefixSP6540TSP6540T2016-09-23
06009696221144VertefixSP6545TSP6545T2016-09-23
06009696221151VertefixSP6550TSP6550T2016-09-23
06009696221175VertefixSP7535TSP7535T2016-09-23
06009696221182VertefixSP7540TSP7540T2016-09-23
06009696221199VertefixSP7545TSP7545T2016-09-23
06009696221205VertefixSP7550TSP7550T2016-09-23
06009696221229VertefixMA5535TMA5535T2016-09-23
06009696221236VertefixMA5540TMA5540T2016-09-23
06009696221243VertefixMA5545TMA5545T2016-09-23
06009696221250VertefixMA5550TMA5550T2016-09-23
06009696221274VertefixMA6535TMA6535T2016-09-23
06009696221281VertefixMA6540TMA6540T2016-09-23
06009696221298VertefixMA6545TMA6545T2016-09-23
06009696221304VertefixMA6550TMA6550T2016-09-23

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Primary DI, Brand, Company table
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