FDA.reportPublic FDA data

Kyocera Medical Technologies, Inc.

Primary DI
00841523117635
Brand
Kyocera Medical Technologies, Inc.
Company
KYOCERA MEDICAL TECHNOLOGIES, INC.
Model
T 710
Catalog number
1706-550-200
Device description
Ti 5.0mm Dia 60mm thread length 200mm total length with Trocar Tip
Published
2015-10-29
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Single use
true

Product Codes#

Code, Name table
CodeName
KTTAppliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KTTAppliance, Fixation, Nail/Blade/Plate Combination, Multiple ComponentOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K110965000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K110965000RENOVIS T 710 LARGE EXTERNAL FIXATION SYSTEMRenovis Surgical Technologies, LLC2011-05-11KTT

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00841523117635PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00841523117635008415231176358415231176350841523117635

GMDN Terms#

Term, Definition table
TermDefinition
External orthopaedic fixation system, single-use, non-sterileAn assembly of non-sterile devices designed to stabilize fractured bones to promote treatment and healing. It typically consists of an external plastic and/or metallic fixator (a framework) and other external and/or implantable components such as clamps, rods, rings, pins, bolts, and nuts, as well as some reusable instrumentation (e.g., wrenches, depth gauge, tensioner). It is used mainly to help the healing of long bones such as the femur, tibia and humerus, as well as fractures of the foot and ankle, joint fusions, and limb lengthening. This is a single-use device intended to be sterilized prior to use.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
116995646
Device count
1
Lot or batch
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00841523146871Kyocera Medical Technologies, Inc.S 1803180-004-0012025-04-08
00841523146888Kyocera Medical Technologies, Inc.S 1803180-004-0022025-04-08
00841523146901Kyocera Medical Technologies, Inc.S 1803180-005-0012025-04-08
00841523146918Kyocera Medical Technologies, Inc.S 1803180-005-0022025-04-08
00841523146932Kyocera Medical Technologies, Inc.S 1803180-006-0002025-04-08
00841523146949Kyocera Medical Technologies, Inc.S 1803180-006-0012025-04-08
00841523146956Kyocera Medical Technologies, Inc.S 1803180-007-0002025-04-08
00841523137060Kyocera Medical Technologies, Inc.S 1281063-730-6172019-01-17
00841523181360Kyocera Medical Technologies, Inc.Tesera-k PL2171-001-0012026-05-26
00841523181681Kyocera Medical Technologies, Inc.Tesera-k PL2171-221-1072026-05-26
00841523181698Kyocera Medical Technologies, Inc.Tesera-k PL2171-221-1082026-05-26
00841523181704Kyocera Medical Technologies, Inc.Tesera-k PL2171-221-1092026-05-26
00841523181711Kyocera Medical Technologies, Inc.Tesera-k PL2171-221-1102026-05-26
00841523181728Kyocera Medical Technologies, Inc.Tesera-k PL2171-221-1112026-05-26
00841523181735Kyocera Medical Technologies, Inc.Tesera-k PL2171-221-1122026-05-26
00841523181742Kyocera Medical Technologies, Inc.Tesera-k PL2171-221-1132026-05-26
00841523181759Kyocera Medical Technologies, Inc.Tesera-k PL2171-221-1142026-05-26
00841523181766Kyocera Medical Technologies, Inc.Tesera-k PL2171-221-1152026-05-26
00841523181773Kyocera Medical Technologies, Inc.Tesera-k PL2171-221-1162026-05-26
00841523181780Kyocera Medical Technologies, Inc.Tesera-k PL2171-229-1072026-05-26

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