The following data is part of a premarket notification filed by Renovis Surgical Technologies, Llc with the FDA for Renovis Cannulated Screw System.
| Device ID | K113084 |
| 510k Number | K113084 |
| Device Name: | RENOVIS CANNULATED SCREW SYSTEM |
| Classification | Screw, Fixation, Bone |
| Applicant | RENOVIS SURGICAL TECHNOLOGIES, LLC 200 HOMER AVE. Ashland, MA 01721 |
| Contact | David F Rothkopf |
| Correspondent | David F Rothkopf RENOVIS SURGICAL TECHNOLOGIES, LLC 200 HOMER AVE. Ashland, MA 01721 |
| Product Code | HWC |
| CFR Regulation Number | 888.3040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-10-18 |
| Decision Date | 2011-12-09 |
| Summary: | summary |