Home GUDID 10381780065494
MBA™ Titanium Subtalar Implant System
Primary DI 10381780065494
Brand MBA™ Titanium Subtalar Implant System
Company Ascension Orthopedics, Inc.
Model 050106
Catalog number 050106
Device description The MBA titanium subtalar implant is cylindrical in shape and incorporates a center cannula designed for use with a guide wire to facilitate proper placement of the implant. The implants are indicated for use in the treatment of the hyperpronated foot and stabilization of the subtalar joint.
Published 2017-10-09
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 Code Name HWC Screw, Fixation, Bone
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class HWC Screw, Fixation, Bone Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 10381780065494 Primary GS1 0 M2480501061 Secondary HIBCC 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized table Source identifier GTIN-14 normalized 10381780065494 10381780065494
GMDN Terms# Term, Definition table Term Definition Subtalar implant, non-bioabsorbable A device designed to be implanted into the calcaneus bone or sinus tarsi of the foot to stabilize the subtalar/talotarsal joint to treat a hyperpronated foot (inward rotation during gait) and sequelae (e.g., flat foot) or other heel/arch abnormalities; it is not intended for arthrodesis/joint fusion. It is a non-bioabsorbable device typically made of a metal (e.g., titanium alloy) or polyethylene (PE).
Device Sizes# Type, Value, Unit table Type Value Unit Device Size Text, specify 0
Storage And Handling# Type, Low, High table Type Low High Condition Special Storage Condition, Specify 0 0 Avoid contact with any objects that may damage the surface finish. Store unopened in respective package until use.
Regulatory Flags# DUNS number 942377524 Device count 1 Lot or batch true Manufacturing date on label true Expiration date on label true Other Devices From This Company# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 03700569658212 Xpert PFP NEWCLIP TECHNICS HWC 2026-06-03 00842188131981 CannCompScrew 2.0mm (SelfDrill) Trimed, INC. HWC 2026-06-02 00842188131998 CannCompScrew 2.0mm (SelfDrill) Trimed, INC. HWC 2026-06-02 00842188132001 CannCompScrew 2.0mm (SelfDrill) Trimed, INC. HWC 2026-06-02 00842188132018 CannCompScrew 2.0mm (SelfDrill) Trimed, INC. HWC 2026-06-02 00842188132025 CannCompScrew 2.0mm (SelfDrill) Trimed, INC. HWC 2026-06-02 00842188132032 CannCompScrew 2.0mm (SelfDrill) Trimed, INC. HWC 2026-06-02 00842188132049 CannCompScrew 2.0mm (SelfDrill) Trimed, INC. HWC 2026-06-02 00842188132056 CannCompScrew 2.0mm (SelfDrill) Trimed, INC. HWC 2026-06-02 00842188132063 Tools - HCS Trimed, INC. HWC 2026-06-02 00842188132070 Tools - HCS Trimed, INC. HWC 2026-06-02 07630894829819 APTUS Medartis AG HWC 2026-06-01 07630894829826 APTUS Medartis AG HWC 2026-06-01 07630894829833 APTUS Medartis AG HWC 2026-06-01 07630894829840 APTUS Medartis AG HWC 2026-06-01 07630894829857 APTUS Medartis AG HWC 2026-06-01 07630894829864 APTUS Medartis AG HWC 2026-06-01 07630894829871 APTUS Medartis AG HWC 2026-06-01 07630894829888 APTUS Medartis AG HWC 2026-06-01 07630894829895 APTUS Medartis AG HWC 2026-06-01 07630894829901 APTUS Medartis AG HWC 2026-06-01 07630894829918 APTUS Medartis AG HWC 2026-06-01 07630894829925 APTUS Medartis AG HWC 2026-06-01 07630894829932 APTUS Medartis AG HWC 2026-06-01 07630894829949 APTUS Medartis AG HWC 2026-06-01 07630894829956 APTUS Medartis AG HWC 2026-06-01 07630894829963 APTUS Medartis AG HWC 2026-06-01 07630894829970 APTUS Medartis AG HWC 2026-06-01 07630894829987 APTUS Medartis AG HWC 2026-06-01 07630894829994 APTUS Medartis AG HWC 2026-06-01