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 |