FDA.reportPublic FDA data

True Tulip Spinal Fixation System

Primary DI
B506L205933850651
Brand
True Tulip Spinal Fixation System
Company
INNOVATIVE SURGICAL DESIGNS
Model
L-205-9-338-5065
Device description
MIS Lordotic Titanium Rods, 5.5 mm x 65 mm
Published
2020-02-11
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
KWPAppliance, Fixation, Spinal Interlaminal
NKBThoracolumbosacral Pedicle Screw System

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KWPAppliance, Fixation, Spinal InterlaminalOrthopedic2
NKBThoracolumbosacral Pedicle Screw SystemOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K181584000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K181584000Redi-SpineInnovative Surgical Designs, Inc.2018-08-10NKB

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
B506L205933850651PrimaryHIBCC0

GMDN Terms#

Term, Definition table
TermDefinition
Bone-screw internal spinal fixation system, sterileAn assembly of 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. Sterile disposable devices associated with implantation may be included.

Sterilization Methods#

Method table
Method
Radiation Sterilization

Regulatory Flags#

DUNS number
078306079
Device count
1
Lot or batch
true
Manufacturing date on label
true
Expiration date on label
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
B50620593085351True Tulip Spinal Fixation System205-9-308-5352020-02-11
B50620593085401True Tulip Spinal Fixation System205-9-308-5402020-02-11
B50620593085451True Tulip Spinal Fixation System205-9-308-5452020-02-11
B50620593085501True Tulip Spinal Fixation System205-9-308-5502020-02-11
B50620593086351True Tulip Spinal Fixation System205-9-308-6352020-02-11
B50620593086401True Tulip Spinal Fixation System205-9-308-6402020-02-11
B50620593086451True Tulip Spinal Fixation System205-9-308-6452020-02-11
B50620593086501True Tulip Spinal Fixation System205-9-308-6502020-02-11
B50620593087351True Tulip Spinal Fixation System205-9-308-7352020-02-11
B50620593087401True Tulip Spinal Fixation System205-9-308-7402020-02-11
B50620593087451True Tulip Spinal Fixation System205-9-308-7452020-02-11
B50620593087501True Tulip Spinal Fixation System205-9-308-7502020-02-11
B506L205933850301True Tulip Spinal Fixation SystemL-205-9-338-50302020-02-11
B506L205933850351True Tulip Spinal Fixation SystemL-205-9-338-50352020-02-11
B506L205933850401True Tulip Spinal Fixation SystemL-205-9-338-50402020-02-11
B506L205933850451True Tulip Spinal Fixation SystemL-205-9-338-50452020-02-11
B506L205933850501True Tulip Spinal Fixation SystemL-205-9-338-50502020-02-11
B506L205933850551True Tulip Spinal Fixation SystemL-205-9-338-50552020-02-11
B506L205933850601True Tulip Spinal Fixation SystemL-205-9-338-50602020-02-11
B506L205933850751True Tulip Spinal Fixation SystemL-205-9-338-50752020-02-11

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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