FDA.reportPublic FDA data

LITe Plate System

Primary DI
07613327066593
Brand
LITe Plate System
Company
Stryker Corporation
Model
49175544
Catalog number
49175544
Device description
REVISION SCREW
Published
2015-09-14
Public version status
Update
Distribution status
Not in Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
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
K142699000
K150449000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K142699000LITe Plate SystemStryker Corporation2014-12-31KWQ
K150449000LITe Plate SystemStryker Corp.2015-03-20KWQ

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
07613327066593PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
07613327066593076133270665937613327066593

GMDN Terms#

Term, Definition table
TermDefinition
Spinal fixation plate, non-bioabsorbableA small, implantable, non-customized sheet of solid material intended to be attached to the spine with screws for spinal immobilization as part of treatment of a spinal instability or deformity; 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). Disposable instruments intended to facilitate implantation, or fixation implants (i.e., bone screws), may be packaged with the plate.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Device Size Text, specify0
Length0

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
149183167
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
07613327665031Sonopet iQ+550026B0105500-26B-0102026-10-12
07613327665048Sonopet iQ+550026B0205500-26B-0202026-10-12
07613327665055Sonopet iQ+550026B1145500-26B-1142026-10-12
07613327665062Sonopet iQ+550026B3125500-26B-3122026-10-12
07613327687149Sonopet iQ+550026B3285500-26B-3282026-10-12
07613327662030ALPHAVENT3911-856-5473911-856-5472025-06-16
07613327662047ALPHAVENT3911-856-5553911-856-5552025-06-16
07613327662054ALPHAVENT3911-856-5653911-856-5652025-06-16
04546540434364SpinePlex04062020000406-202-0002016-06-30
07613252254430VertaPlex04066220000406-622-0002016-09-23
07613327141788SpinePlex04062020100406-202-0102016-09-23
07613154757091VertaPlex04064020000406-402-0002016-06-30
07613327141764VertaPlex04064020020406-402-0022016-09-23
07613327170559VertaPlex HV04066220150406-622-0152016-09-23
07613327170566VertaPlex04064020150406-402-0152016-09-23
00808232000214NA2102-01312102-01312015-09-24
07613327124200Vitoss VBA Pack2102-24012102-24012015-12-09
07613327124217Vitoss VBA Pack2101-24052102-24052015-12-09
07613327124224Vitoss VBA Pack2102-24022102-24022015-12-09
07613327124231Vitoss VBA Pack2102-24102102-24102015-12-09

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