Primary Device ID | 03613720192244 |
NIH Device Record Key | 1829b665-5aea-495f-8ad8-ade2694e9f49 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | K-JAWS |
Version Model Number | B10121714 |
Company DUNS | 383228632 |
Company Name | MEDICREA INTERNATIONAL |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03613720192244 [Primary] |
PHQ | Anterior Staple As Supplemental Fixation For Fusion |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2021-11-23 |
Device Publish Date | 2015-10-23 |
03613720192282 | ANTERIOR CERVICAL STABILIZATION H: 20mm x L: 17mm |
03613720192275 | ANTERIOR CERVICAL STABILIZATION H: 20mm x L: 14mm |
03613720192268 | ANTERIOR CERVICAL STABILIZATION H: 20mm x L: 12mm |
03613720192251 | ANTERIOR CERVICAL STABILIZATION H: 17.5mm x L: 17mm |
03613720192244 | ANTERIOR CERVICAL STABILIZATION H: 17.5mm x L: 14mm |
03613720192237 | ANTERIOR CERVICAL STABILIZATION H: 17.5mm x L: 12mm |
03613720192220 | ANTERIOR CERVICAL STABILIZATION H: 15mm x L: 17mm |
03613720192213 | ANTERIOR CERVICAL STABILIZATION H: 15mm x L: 14mm |
03613720192206 | ANTERIOR CERVICAL STABILIZATION H: 15mm x L: 12mm |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() K-JAWS 79072217 3744965 Live/Registered |
MEDICREA INTERNATIONAL 2009-04-15 |