ZB Z1 Guide
ZB Z1 Guide
Surgical Technique
INTENDED USE
INDICATIONS CONTRAINDICATIONS
1. Advanced wear of the joint due to degenerative, 1. Acute, chronic, local, or systemic infections.
post-traumatic or rheumatic diseases. 2. Severe muscular, neural, or vascular diseases
2. Failed previous hip surgery including joint that endanger the limbs involved.
reconstruction (osteotomy), arthrodesis, hemi- 3. Lack of bony structures proximal or distal to the
arthroplasty or total hip replacement (THR). joint, so that good anchorage of the implant is
3. Acute traumatic fracture of the femoral head or unlikely or impossible.
neck. 4. Total or partial absence of the muscular or
4. Avascular necrosis of the femoral head. ligamentous apparatus.
5. Any concomitant diseases that can jeopardize
the functioning and the success of the implant.
6. Allergy to the implanted material, especially to
metal (e. g., cobalt, chromium, nickel, etc.).
7. Local bone tumors and/or cysts.
8. Pregnancy.
9. Skeletal immaturity.
Table of Contents
System Overview....................................................................................................... 2
Pre-operative Planning.............................................................................................. 3
Calcar Preparation..................................................................................................... 6
Trial Reduction........................................................................................................... 7
Head Impaction......................................................................................................... 9
Step 7: Step 8:
Femoral Implant Insertion Femoral Implant Insertion
2 | Z1™ Hip System Surgical Technique
System Overview
The Z1 Hip System includes two different implant
bodies.
• Cementless Collared,
• Cementless Collarless,
Figure 1 Figure 2
The Z1 Hip System provides X-ray templates with Once the correct magnification has been established,
100%, 110%, 115%, and 120% magnification the digital templating system can be used to determine
(Figure 1). It is recommended to use a radiographic the optimal implant size and center of rotation
marker to assess the X-ray magnification and select (Figure 2).
the appropriate template. It is also recommended that
templates are positioned over the AP X-rays to best
decide the correct implant size and center of rotation.
4 | Z1™ Hip System Surgical Technique
Figure 3 Figure 4
Patient Positioning/
Surgical Exposure Femoral Neck Resection
The Z1 Hip System femoral components can be Depending on the surgeon’s preference and surgical
implanted using any of the standard approaches for approach, the neck cut can be made prior to or after
total or hemi hip replacement (Figure 3). dislocation. The neck cut can also be made at different
heights in line with the surgeon’s preoperative plan
(Figure 4).
5 | Z1™ Hip System Surgical Technique
Figure 12 Figure 13
Trial Reduction
With the final broach in place, select the appropriate Once the provisional neck is in place, select the
provisional neck (Standard Offset, High Offset or Coxa correct provisional head size and position it onto
Vara) and assemble it onto the broach (Figure 12). the provisional neck (Figure 13). Perform the trial
reduction and if necessary, repeat the procedure with
Color Coding – Stem Variant different head offsets.
Gold Standard Offset (STD) (135˚)
Note: There is a 3.5 mm increase in neck lengths
Black High Offset (HO) (135˚)
between the core sizes (0 to 9) and macro sizes (10
Silver Coxa Vara (CV) (126.5˚)
to 12).
6mm
Horizontal Offset – Horizontal offset: 6 mm shift between STD and HO
or Coxa Vara.
Figure 15 Figure 16
Notes
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intellectual property rights, as applicable, owned by or licensed to
Zimmer Biomet or its affiliates unless otherwise indicated, and must not
be redistributed, duplicated or disclosed, in whole or in part, without the
express written consent of Zimmer Biomet.
This material is intended for health care professionals. Distribution to any
other recipient is prohibited.
For product information, including indications, contraindications,
warnings, precautions, potential adverse effects and patient counseling
information, see the package insert and www.zimmerbiomet.com.
Please refer to the Instructions for Use and the package insert to the
products to be used with this Surgical Technique.
Zimmer Biomet does not practice medicine. This technique was
developed in conjunction with health care professionals. This document
is intended for surgeons and is not intended for laypersons. Each surgeon
should exercise his or her own independent judgment in the diagnosis
and treatment of an individual patient, and this information does not
purport to replace the comprehensive training surgeons have received.
As with all surgical procedures, the technique used in each case will
depend on the surgeon’s medical judgment as the best treatment for
each patient. Results will vary based on health, weight, activity and
other variables. Not all patients are candidates for this product and/or
procedure.
Caution: Federal (USA) law restricts this device to sale by or on the order
of a physician. Rx only.
For Ordering Information please refer to document 4740.X-US-en.
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USA