The following data is part of a premarket notification filed by Titan Spine, Llc with the FDA for Endoskeleton; Ta Ibd And Vbr, To And Tt, Tas, Tc, Tl.
| Device ID | K141953 |
| 510k Number | K141953 |
| Device Name: | ENDOSKELETON; TA IBD AND VBR, TO AND TT, TAS, TC, TL |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | TITAN SPINE, LLC 3416 ROXEE RUN COVE Bartlett, TN 38133 |
| Contact | Christine Scifert |
| Correspondent | Christine Scifert TITAN SPINE, LLC 3416 ROXEE RUN COVE Bartlett, TN 38133 |
| Product Code | MAX |
| Subsequent Product Code | MQP |
| Subsequent Product Code | ODP |
| Subsequent Product Code | OVD |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-07-18 |
| Decision Date | 2014-10-27 |
| Summary: | summary |