Primary Device ID | 00811714034164 |
NIH Device Record Key | e2c3e7ec-a58e-4b84-9878-e56062399a5c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Spirit PEEK Screw |
Version Model Number | 900000-1135 |
Catalog Number | 900000-1135 |
Company DUNS | 002745858 |
Company Name | RESPONSIVE ORTHOPEDICS 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 | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00811714034164 [Primary] |
HWC | Screw, Fixation, Bone |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-05-06 |
Device Publish Date | 2021-04-28 |
00811714034164 | 900000-1135 |
00811714034096 | 900000-1128 |
00811714034041 | 900000-1123 |
00811714034003 | 900000-1035 |
00811714033938 | 900000-1028 |
00811714033884 | 900000-1023 |
00811714033846 | 900000-0935 |
00811714033778 | 900000-0928 |
00811714033723 | 900000-0923 |
00811714033686 | 900000-0835 |
00811714033617 | 900000-0828 |
00811714033563 | 900000-0823 |
00811714033525 | 900000-0735 |
00811714033457 | 900000-0728 |
00811714033402 | 900000-0723 |