PLS

Primary DI
00810086191055
Brand
PLS
Company
SINTEA USA, LLC
Model
PLS-555T56
Device description
Dual Lead Screw Ø6 L55mm
Published
2024-12-04
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
KWPAppliance, Fixation, Spinal Interlaminal

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KWPAppliance, Fixation, Spinal InterlaminalOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K140787000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K140787000PLS (POSTERIOR LUMBAR SYSTEM)Sintea Plustek, LLC2014-05-30MNH

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00810086191055PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00810086191055008100861910558100861910550810086191055

GMDN Terms#

Term, Definition table
TermDefinition
Bone-screw internal spinal fixation system rodAn implantable component of a bone-screw internal spinal fixation system in the form of a thin cylinder intended to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities, and also used as an adjunct to spinal fusion [e.g., for degenerative disc disease (DDD)]. This component is designed as a longitudinal (intervertebral) connecting element passing through the system’s implantable screw heads or hooks. It is available in various forms (e.g., straight, curved, rigid, flexible, with varying diameters); flexible types may allow small movements of the spine.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
3054906850info@sinteausa.com

Regulatory Flags#

DUNS number
079917057
Device count
1
Lot or batch
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00810086190720PLSPLS-540T5402024-12-06
00810086190706PLSPLS-530T5402024-12-04
00810086190713PLSPLS-535T5402024-12-04
00810086190737PLSPLS-545T5402024-12-04
00810086190874PLSPLS-540T552024-12-04
00810086190881PLSPLS-545T552024-12-04
00810086190898PLSPLS-550T552024-12-04
00810086191000PLSPLS-530T562024-12-04
00810086191154PLSPLS-530T572024-12-04
00810086191161PLSPLS-535T572024-12-04
00810086193394PLSPLS-845T562024-12-04
00810086193400PLSPLS-850T562024-12-04
00810086193547PLSPLS-845T572024-12-04
00810086193554PLSPLS-850T572024-12-04
00810086193691PLSPLS-845T582024-12-04
00810086193714PLSPLS-855T582024-12-04
00810086190867PLSPLS-535T552024-09-19

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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00840606186551OMEGA XPSPINAL ELEMENTS, INC.KWP2026-09-22
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10888857598171Xia® 3 System - Serrato®VB Spine LLCKWP2026-07-24
10888857598188Xia® 3 System - Serrato®VB Spine LLCKWP2026-07-24
10888857598195Xia® 3 System - Serrato®VB Spine LLCKWP2026-07-24
10888857598201Xia® 3 System - Serrato®VB Spine LLCKWP2026-07-24
10888857598218Xia® 3 System - Serrato®VB Spine LLCKWP2026-07-24
10888857598225Xia® 3 System - Serrato®VB Spine LLCKWP2026-07-24
10888857598232Xia® 3 System - Serrato®VB Spine LLCKWP2026-07-24
10888857598249Xia® 3 System - Serrato®VB Spine LLCKWP2026-07-24
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04546540148025XIA IIStryker CorporationKWP2014-12-08