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 |