| Primary Device ID | B565FO20132090 |
| NIH Device Record Key | f9b026f3-7f6d-460c-8ae1-5c92386ec9b4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Orbitum X Staple |
| Version Model Number | FO-2013-209 |
| Catalog Number | FO-2013-209 |
| Company DUNS | 017138000 |
| Company Name | CPM MEDICAL CONSULTANTS, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| 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 | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | true |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx | |
| Phone | 972-331-5860 |
| xx@xx.xx |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | B565FO20132090 [Primary] |
| JDR | Staple, Fixation, Bone |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
[B565FO20132090]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-01-28 |
| Device Publish Date | 2025-01-20 |
| B565FO100020120 | 20mm Round Staple |
| B565FO100016100 | 16mm Round Staple |
| B565FO100012080 | 12mm Round Staple |
| B565FO100024160 | 24mm VI Hourglass Staple |
| B565FO100024140 | 24mm Round Staple |
| B565FO100124140 | Orbitum X Round Staple Implant 24MM |
| B565FO2021241 | 24MM PLANER |
| B565FO20132090 | 2.0 MM K-WIRE, 9 INCH Guide wire Trocar |