Primary Device ID | 00817906022780 |
NIH Device Record Key | 4a309151-a5f0-49c5-960e-cdc9d5c6cded |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Fracture and Correction CoLag™ |
Version Model Number | P65 ST112 |
Company DUNS | 079700711 |
Company Name | IN2BONES USA, 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 | 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 | 00817906022780 [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 | 2018-09-06 |
Device Publish Date | 2018-08-06 |
00817906022919 | SCREW, Ø2.5X10.0 mm |
00817906022902 | SCREW, Ø2.5X8.0 mm |
00817906022896 | SCREW, Ø2.0X30.0 mm |
00817906022889 | SCREW, Ø2.0X28.0 mm |
00817906022872 | SCREW, Ø2.0X26.0 mm |
00817906022865 | SCREW, Ø2.0X24.0 mm |
00817906022858 | SCREW, Ø2.0X22.0 mm |
00817906022841 | SCREW, Ø2.0X20.0 mm |
00817906022834 | SCREW, Ø2.0X18.0 mm |
00817906022827 | SCREW, Ø2.0X16.0 mm |
00817906022810 | SCREW, Ø2.0X15.0 mm |
00817906022803 | SCREW, Ø2.0X14.0 mm |
00817906022797 | SCREW, Ø2.0X13.0 mm |
00817906022780 | SCREW, Ø2.0X12.0 mm |
00817906022773 | SCREW, Ø2.0X11.0 mm |
00817906022766 | SCREW, Ø2.0X10.0 mm |
00817906022759 | SCREW, Ø2.0X9.0 mm |
00817906022742 | SCREW, Ø2.0X8.0 mm |