Primary Device ID | 00840019908870 |
NIH Device Record Key | 1cd2e04e-45e3-4f2d-9445-09e11f824d9e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ShurFit CRT Peek Cage |
Version Model Number | CRTP10-09 |
Catalog Number | CRTP10-09 |
Company DUNS | 079398589 |
Company Name | PRECISION SPINE, INC. |
Device Count | 1 |
DM Exempt | true |
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 | false |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840019908870 [Primary] |
JDK | Prosthesis, Hip, Cement Restrictor |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00840019908870]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2020-02-24 |
Device Publish Date | 2019-04-12 |
00840019908900 | CRT Peek 10 degree x 12mm |
00840019908894 | CRT Peek 10 degree x 11mm |
00840019908887 | CRT Peek 10 degree x 10mm |
00840019908870 | CRT Peek 10 degree x 09mm |
00840019908863 | CRT Peek 10 degree x 08mm |
00840019908856 | CRT Peek 10 degree x 07mm |
00840019908849 | CRT Peek 10 degree x 06mm |
00840019908832 | CRT Peek 10 degree x 05mm |
00840019908825 | CRT Peek 5 degree x 12mm |
00840019908818 | CRT Peek 5 degree x 11mm |
00840019908801 | CRT Peek 5 degree x 10mm |
00840019908795 | CRT Peek 5 degree x 9mm |
00840019908788 | CRT Peek 5 degree x 8mm |
00840019908771 | CRT Peek 5 degree x 7mm |
00840019908764 | CRT Peek 5 degree x 6mm |
00840019908757 | CRT Peek 5 degree x 5mm |