| Primary Device ID | 20841019109520 |
| NIH Device Record Key | 173cc385-6153-49f8-8464-577aae32959c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Precision Spine |
| Version Model Number | 54-BP-5000 |
| Company DUNS | 151352023 |
| Company Name | Precision Spine |
| 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 | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | 781-834-9500 |
| kprario@ksp.com |
| Length | 8 Inch |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00841019109526 [Primary] |
| GS1 | 10841019109523 [Package] Contains: 00841019109526 Package: [1 Units] In Commercial Distribution |
| GS1 | 20841019109520 [Package] Contains: 00841019109526 Package: [5 Units] In Commercial Distribution |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[20841019109520]
Radiation Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-07-10 |
| 20841019109520 | Bipolar Coagulation Forceps 8" (20.3cm) Working Length Hardy Bayonet Insulated, 1mm Tip |
| 00841019109519 | Bipolar Coagulation Forceps 8" (20.3cm) Working Length Cushing Bayonet Insulated, 1mm Tip |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PRECISION SPINE 85583289 4973366 Live/Registered |
SPINAL USA, INC. 2012-03-29 |
![]() PRECISION SPINE 78715318 not registered Dead/Abandoned |
Michael James Davis Sr 2005-09-19 |