Home GUDID 07613327122077
OASYS
Primary DI 07613327122077
Brand OASYS
Company Stryker Corporation
Model 48554352
Catalog number 48554352
Device description BONE 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
Single use true Product Codes# Code, Name table Code Name KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL MRW SYSTEM, FACET SCREW SPINAL DEVICE
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class KWP Appliance, Fixation, Spinal Interlaminal Orthopedic 2 MRW System, Facet Screw Spinal Device Unknown U
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 07613327122077 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 07613327122077 07613327122077 7613327122077
GMDN Terms# Term, Definition table Term Definition Bone-screw internal spinal fixation system, non-sterile An 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.
Device Sizes# Type, Value, Unit table Type Value Unit Device Size Text, specify 0 Length 52 Millimeter
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 149183167 Device count 1 Lot or batch true Manufacturing date on label true Sterilization required before use true Other Devices From This Company# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 00840466901035 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901042 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901059 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901066 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901073 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901080 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901097 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901103 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901110 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901127 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901141 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901158 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901165 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901172 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901479 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901486 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901493 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901509 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901516 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901523 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901530 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901547 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901554 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901561 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901578 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901585 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901592 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901608 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901615 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21 00840466901622 Primus SPINAL ELEMENTS, INC. KWP 2026-07-21