ICD-10-PCS Billable Code

0PU80JZ

Supplement Glenoid Cavity, Left to No Qualifier with Synthetic Substitute, Open Approach

Procedural Specifications

Clinical Axis Detail Definition
Section0 Medical and Surgical
Body SystemP Upper Bones
OperationU Supplement
Body Part8 Glenoid Cavity, Left
Approach0 Open
DeviceJ Synthetic Substitute
QualifierZ No Qualifier

Operation Definition

Putting in or on biological or synthetic material that physically reinforces and/or augments the function of a portion of a body part

Procedure Overview

Supplement procedures add biological or synthetic material to reinforce or augment a bone of the skull, face, thorax, or upper limb that remains anatomically in place, rather than replacing or repairing damaged tissue. Common examples include bone grafting to reinforce a weakened area of the skull, or augmenting a thin area of the sternum or scapula with mesh or cement to add structural strength.

This approach is chosen when the native bone is largely intact and functional but needs extra support, often to prevent future fracture, to build up bone stock before another procedure, or to strengthen a surgical repair site.

Anatomy & Axis Detail

Glenoid Cavity, Left

The left glenoid cavity forms the socket half of the shoulder joint, and its depth and orientation determine how well the humeral head stays centered during arm movement. When bone loss from chronic instability, glenohumeral arthritis, or revision arthroplasty erodes this socket, the joint can become unstable or unsuitable for standard implant fixation. Supplement addresses this by adding bone graft or an augmenting device to rebuild lost glenoid volume and restore a stable articulating surface, a step often required before or during shoulder replacement or stabilization surgery. Because the amount and pattern of bone loss vary widely between patients, documentation should capture the graft type and the extent of the glenoid reconstructed on this left side.

Approach: Open

Open approach means the surgeon cuts through skin, mucous membrane, or other tissue layers to physically expose the target site to view before performing the procedure. It gives direct visualization and hands-on access, distinguishing it from Percutaneous approaches where instruments pass through a small puncture without exposing the site. Open is typical for procedures needing wide access, such as most laparotomies.

Device: Synthetic Substitute

Synthetic Substitute designates a device made from manufactured, non-biologic material, such as mesh or prosthetic components, used to replace or augment a body part. It is distinguished from the two tissue substitute categories by its artificial composition, which carries different considerations for integration and long-term durability than biologic grafts.

Coding & Documentation

Coders should confirm the operative note describes material being added to reinforce a structure that stays in place, not material substituting for a removed part. The device or graft type documented determines the correct device value - autograft, allograft, synthetic substitute, or nonautologous tissue - so vague documentation of "bone graft" without a source can complicate accurate coding. A common mistake is coding supplement when the surgeon actually performed a replacement, particularly in cranioplasty cases where it's unclear whether native bone was removed first. Another frequent error is missing a supplement code entirely when a graft was placed during a repair or reposition procedure, since it may require a separate code rather than being bundled in.

Commonly Confused With

ReplacementReplacement is the closest match and the two are distinguished by whether the original bone was removed - supplement reinforces bone left in place, while replacement requires a body part to be taken out before the substitute goes in.
RepairRepair can also overlap since both may involve grafting, but repair is coded when the graft is restoring a structural defect rather than adding reinforcing bulk to an already intact structure.