Primary Device ID | M69520502P2610810S0 |
NIH Device Record Key | 2059b30a-625c-4d05-9511-6e6323a9c654 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PLIF Interbody System |
Version Model Number | 20-502-P2610810-S |
Catalog Number | 20-502-P2610810-S |
Company DUNS | 010968002 |
Company Name | Tyber Medical 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 |
Phone | +1(866)761-0933 |
jstigliano@tybermed.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | M69520502P2610810S0 [Primary] |
MAX | Intervertebral fusion device with bone graft, lumbar |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2020-02-24 |
Device Publish Date | 2019-11-12 |
M69520502P269810S0 | PLIF TiPEEK 26mm x 10mm x 9mm x 8 deg |
M69520502P26888S0 | PLIF TiPEEK 26mm x 8mm x 8mm x 8 deg |
M69520502P268810S0 | PLIF TiPEEK 26mm x 10mm x 8mm x 8 deg |
M69520502P267810S0 | PLIF TiPEEK 26mm x 10mm x 7mm x 8 deg |
M69520502P2612810S0 | PLIF TiPEEK 26mm x 10mm x 12mm x 8 deg |
M69520502P2611810S0 | PLIF TiPEEK 26mm x 10mm x 11mm x 8 deg |
M69520502P2610810S0 | PLIF TiPEEK 26mm x 10mm x 10mm x 8 deg |
M69520502P24988S0 | PLIF TiPEEK 24mm x 8mm x 9mm x 8 deg |
M69520502P241488S0 | PLIF TiPEEK 24mm x 8mm x 14mm x 8 deg |
M69520502P241388S0 | PLIF TiPEEK 24mm x 8mm x 13mm x 8 deg |
M69520502P241288S0 | PLIF TiPEEK 24mm x 8mm x 12mm x 8 deg |
M69520502P241088S0 | PLIF TiPEEK 24mm x 8mm x 10mm x 8 deg |