| Primary Device ID | 00880304993563 |
| NIH Device Record Key | 330d7ebc-eab3-4a87-922b-5cc9916891e4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | M2a Magnum™ Hip System |
| Version Model Number | US157864 |
| Catalog Number | US157864 |
| Company DUNS | 129278169 |
| Company Name | Biomet Orthopedics, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00880304993563 [Primary] |
| KWY | Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-05-05 |
| Device Publish Date | 2017-10-06 |
| 00880304993693 | US257866 |
| 00880304993686 | US257864 |
| 00880304993679 | US257862 |
| 00880304993662 | US257860 |
| 00880304993655 | US257858 |
| 00880304993648 | US257856 |
| 00880304993631 | US257854 |
| 00880304993624 | US257852 |
| 00880304993617 | US257850 |
| 00880304993600 | US257848 |
| 00880304993594 | US257846 |
| 00880304993587 | US257844 |
| 00880304993570 | US157866 |
| 00880304993563 | US157864 |
| 00880304993556 | US157862 |
| 00880304993549 | US157860 |
| 00880304993532 | US157858 |
| 00880304993525 | US157856 |
| 00880304993518 | US157854 |
| 00880304993501 | US157852 |
| 00880304993495 | US157850 |
| 00880304993488 | US157848 |
| 00880304993471 | US157846 |
| 00880304993464 | US157844 |