The OVOMotion™ Shoulder Arthroplasty System includes:
1. Humeral articular component and a taper post fixation component that mate together via a taper interlock to provide stable and immobile fixation of the implant and stress bearing contact at the bone/prosthetic interface;
2. Glenoid resurfacing component intended to articulate with the humeral component when both articular surfaces of the shoulder joint are affected.
The enclosed humeral articular component may be used with an appropriate Arthrosurface glenoid component (sold separately).
Materials Articular Component: Cobalt-Chronium Alloy (Co-Cr-Mo)
Undersurface Coating: Titanium (CPTi)
Taper Post: Titanium Alloy (Ti-6Al-4V)
Indications
For the reconstruction of painful and/or severely disabled shoulder joints resulting from posttraumatic degenerative disease or avascular necrosis. The humeral head and neck and glenoid vault should be of sufficient bone stock to support loading. The rotator cuff should be intact or reconstructible.
The device is a single use implant intended to be used for hemiarthroplasty or in conjunction with the Arthrosurface glenoid component for total shoulder arthroplasty.
Both humeral and glenoid components of the OVOMotion™ Shoulder Arthroplasty System are intended for cemented use only.
MED&CARE Sp. z o.o.
ul. Mławska 13
81-204 Gdynia, Poland
NIP 9581708968
REGON 386298925
phone: +48 58 776 22 75
fax: +48 58 350 97 57
mobile: +48 506 399 272
email: office@medandcare.pl
Number: PL 92 1020 1853 0000 9502 0124 1017
Bank PKO BP SA, I Oddział w Gdyni
Kod BIC (Swift): BPKOPLPW
Severity: Notice
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