The following data is part of a premarket notification filed by Renovis Surgical Technologies, Llc with the FDA for S128 Anterior Lumbar Interbody Fusion (alif) System.
| Device ID | K131122 |
| 510k Number | K131122 |
| Device Name: | S128 ANTERIOR LUMBAR INTERBODY FUSION (ALIF) SYSTEM |
| Classification | Intervertebral Fusion Device With Integrated Fixation, Lumbar |
| Applicant | RENOVIS SURGICAL TECHNOLOGIES, LLC 200 Homer Ave Ashland, MA 01721 |
| Contact | Sharyn Orton, Ph.d. |
| Correspondent | Sharyn Orton, Ph.d. RENOVIS SURGICAL TECHNOLOGIES, LLC 200 Homer Ave Ashland, MA 01721 |
| Product Code | OVD |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-04-22 |
| Decision Date | 2013-09-18 |
| Summary: | summary |