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 |