Primary Device ID | 00810482030415 |
NIH Device Record Key | d2c6a4e8-40f2-4635-a131-3d55827a8c4f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Blustone Synergy Lumbar Interbody Fusion System (Basalt) |
Version Model Number | 2410-PL14 |
Company DUNS | 033467608 |
Company Name | BLUSTONE SYNERGY, 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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
00810482030453 | The Blustone Synergy Lumbar Interbody Fusion System (Basalt) may be implanted:
- bi-laterally in |
00810482030446 | The Blustone Synergy Lumbar Interbody Fusion System (Basalt) may be implanted:
- bi-laterally in |
00810482030439 | The Blustone Synergy Lumbar Interbody Fusion System (Basalt) may be implanted:
- bi-laterally in |
00810482030422 | The Blustone Synergy Lumbar Interbody Fusion System (Basalt) may be implanted:
- bi-laterally in |
00810482030415 | The Blustone Synergy Lumbar Interbody Fusion System (Basalt) may be implanted:
- bi-laterally in |
00810482030408 | The Blustone Synergy Lumbar Interbody Fusion System (Basalt) may be implanted:
- bi-laterally in |
00810482030392 | The Blustone Synergy Lumbar Interbody Fusion System (Basalt) may be implanted:
- bi-laterally in |
00810482030385 | The Blustone Synergy Lumbar Interbody Fusion System (Basalt) may be implanted:
- bi-laterally in |
00810482030378 | .The Blustone Synergy Lumbar Interbody Fusion System (Basalt) may be implanted:
- bi-laterally i |