SpaceFlex Shoulder

"Disposable cement spacer molds with metal reinforcement stem are indicated for use to mold a temporary hemi- shoulder replacement for skeletally mature patients undergoing a two-stage…

Registry build 21.09.26

“Disposable cement spacer molds with metal reinforcement stem are indicated for use to mold a temporary hemi- shoulder replacement for skeletally mature patients undergoing a two-stage revision procedure due to a septic process. The temporary prosthesis is molded using low viscosity polymethylmethacrylate bone cement and inserted into the humeral medullary canal and glenoid cavity of the shoulder following removal of the existing humeral and glenoideal cavity implants and debridement. SpaceFlex Shoulder should only be used with G3A low-viscosity bone cement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). The hemi-shoulder prosthesis made from the SpaceFlex Shoulder disposable cement molds is not intended for use more than 180 days, at which time it must be explanted and permanent devices implanted or another appropriate treatment performed (e.g. resection arthroplasty, fusion, etc.). Due to the inherent mechanical limitations of the hemi-shoulder prosthesis material (low viscosity polymethylmethacrylate), the temporary hemi-shoulder prosthesis is only indicated for patients who will consistently follow activity limitation throughout the implant period. The device can exclusively be used by competent healthcare personnel who has complete scientific and anatomical knowledge.”

1manufacturer
6catalogue numbers in this listing

Who Else Makes It

Registered in Shanghai.

Chinese manufacturers registered for FDA product code MBB
Manufacturer City Province Registered as Device types
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106

Record

Regulatory record for SpaceFlex Shoulder
Listed by G21 SRL
FDA product code MBB
Device type Bone Cement, Antibiotic
Device class Class 2
Regulation 21 CFR 888.3027
510(k) K202338
Record published 2021-03-05

Specifications

Specifications
MRI safety MR Unsafe
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Storage Handling environment temperature 50 to 104 °F

Catalogue Numbers

Catalogue numbers for SpaceFlex Shoulder
Catalogue number Size Status
900001 124215 In distribution
900001 084215 In distribution
900001 124818 In distribution
900001 144818 In distribution
900001 104818 In distribution
900001 104215 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Remedy Spacer Osteoremedies, LLC 28
CeMend Shoulder Spacer Mold G21 SRL 12
Palacos® Heraeus Medical LLC 8
StageOne™ Biomet Orthopedics 8
Interspace Tapered Wedge Stem Tecres SPA 6
InterSpace Hip Tecres SPA 6
Surespace Ortho Development Corp. 5
Prostalac Depuy Orthopaedics, Inc. 4
CeMend Shoulder Spacer G21 SRL 4
Rally Smith & Nephew, Inc. 3
Smartset Depuy (Ireland) 3
SpaceFlex Knee G21 SRL 3

Showing 12 of 44. All products under Bone Cement, Antibiotic

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer