The following data is part of a premarket notification filed by Spinecraft with the FDA for Orio-c Cervical, Orio-tl Tlif, Orio-pl Plif, Orio-al Alif Intervedrtebral Body Fusion Cages.
| Device ID | K090887 |
| 510k Number | K090887 |
| Device Name: | ORIO-C CERVICAL, ORIO-TL TLIF, ORIO-PL PLIF, ORIO-AL ALIF INTERVEDRTEBRAL BODY FUSION CAGES |
| Classification | Intervertebral Fusion Device With Bone Graft, Cervical |
| Applicant | SPINECRAFT 1001 OAKWOOD BLVD. Round Rock, TX 78681 |
| Contact | J.d. Webb |
| Correspondent | J.d. Webb SPINECRAFT 1001 OAKWOOD BLVD. Round Rock, TX 78681 |
| Product Code | ODP |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-03-31 |
| Decision Date | 2009-10-30 |
| Summary: | summary |