FDA.reportPublic FDA data

PCT

Primary DI
00815101024318
Brand
PCT
Company
Centinel Spine, LLC
Model
PCT0135044
Published
2017-01-30
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
KWPAppliance, Fixation, Spinal Interlaminal
NKGOrthosis, Cervical Pedicle Screw Spinal Fixation

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KWPAppliance, Fixation, Spinal InterlaminalOrthopedic2
NKGPosterior Cervical Screw SystemOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K152211000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K152211000PCT SystemCentinel Spine, Inc.2015-12-01NKG

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00815101024318PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00815101024318008151010243188151010243180815101024318

GMDN Terms#

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

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
949024850
Device count
1
Lot or batch
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00843193111838Prodisc L InstrumentPDL1182026-06-08
00843193112323Prodisc C, SK, Vivo, Nova Instrument03.820.102.02S-CS2026-06-08
00843193112330Prodisc C, SK, Vivo, Nova Instrument03.820.103.02S-CS2026-06-08
00843193112347Prodisc C, SK, Vivo, Nova Instrument03.820.104.02S-CS2026-06-08
00843193112354Prodisc C, SK, Vivo, Nova Instrument03.820.105.02S-CS2026-06-08
00843193112361Prodisc C, SK, Vivo, Nova Instrument03.820.110.02S-CS2026-06-08
00843193119926Prodisc C, SK, Vivo, Nova Instrument03.820.102-CS2026-06-08
00843193119933Prodisc C, SK, Vivo, Nova Instrument03.820.103-CS2026-06-08
00843193119940Prodisc C, SK, Vivo, Nova Instrument03.820.104-CS2026-06-08
00843193119957Prodisc C, SK, Vivo, Nova Instrument03.820.105-CS2026-06-08
00843193119964Prodisc C, SK, Vivo, Nova Instrument03.820.106-CS2026-06-08
00843193119971Prodisc C, SK, Vivo, Nova Instrument03.820.107-CS2026-06-08
00843193119988Prodisc C, SK, Vivo, Nova Instrument03.820.108-CS2026-06-08
00843193119995Prodisc C, SK, Vivo, Nova Instrument03.820.109-CS2026-06-08
00843193120007Prodisc C, SK, Vivo, Nova Instrument03.820.110-CS2026-06-08
00843193111708Prodisc LPDL-L-PT10S2018-10-16
00843193111715Prodisc LPDL-L-PT12S2018-10-16
00843193111722Prodisc LPDL-L-PT14S2018-10-16
00843193111739Prodisc LPDL-L-SP06S2018-10-16
00843193111746Prodisc LPDL-L-SP11S2018-10-16

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
04052536162109neon3Ulrich GmbH & Co. KGNKG2026-06-08
04052536162109neon3Ulrich GmbH & Co. KGKWP2026-06-08
04052536162123neon3Ulrich GmbH & Co. KGKWP2026-06-08
04052536162123neon3Ulrich GmbH & Co. KGNKG2026-06-08
04052536162185neon3Ulrich GmbH & Co. KGKWP2026-06-08
04052536162185neon3Ulrich GmbH & Co. KGNKG2026-06-08
04052536162192neon3Ulrich GmbH & Co. KGKWP2026-06-08
04052536162192neon3Ulrich GmbH & Co. KGNKG2026-06-08
04052536162208neon3Ulrich GmbH & Co. KGKWP2026-06-08
04052536162208neon3Ulrich GmbH & Co. KGNKG2026-06-08
04052536194285neon3Ulrich GmbH & Co. KGKWP2026-06-08
04052536194285neon3Ulrich GmbH & Co. KGNKG2026-06-08
04052536194292neon3Ulrich GmbH & Co. KGKWP2026-06-08
04052536194292neon3Ulrich GmbH & Co. KGNKG2026-06-08
04052536194308neon3Ulrich GmbH & Co. KGNKG2026-06-08
04052536194308neon3Ulrich GmbH & Co. KGKWP2026-06-08
00197157082031ZAVATION SCREWZavation LLCKWP2026-06-05
00197157082048ZAVATION SCREWZavation LLCKWP2026-06-05
00197157082055ZAVATION SCREWZavation LLCKWP2026-06-05
00197157082062ZAVATION SCREWZavation LLCKWP2026-06-05
00197157082079ZAVATION SCREWZavation LLCKWP2026-06-05
00197157082086ZAVATION SCREWZavation LLCKWP2026-06-05
00197157082093ZAVATION SCREWZavation LLCKWP2026-06-05
00197157082109ZAVATION SCREWZavation LLCKWP2026-06-05
00197157082116ZAVATION SCREWZavation LLCKWP2026-06-05
00197157082123ZAVATION SCREWZavation LLCKWP2026-06-05
00840283403897VySpan™VY SPINE LLCKWP2026-06-05
00840283403897VySpan™VY SPINE LLCNKG2026-06-05
00840283403927VySpan™VY SPINE LLCKWP2026-06-05
00840283403927VySpan™VY SPINE LLCNKG2026-06-05