The following data is part of a premarket notification filed by Renovis Surgical Technologies, Llc with the FDA for S 100 Pedicle Screw System.
Device ID | K101682 |
510k Number | K101682 |
Device Name: | S 100 PEDICLE SCREW SYSTEM |
Classification | Orthosis, Spinal Pedicle Fixation |
Applicant | RENOVIS SURGICAL TECHNOLOGIES, LLC 1001 OAKWOOD BLVD Round Rock, TX 78681 |
Contact | J.d. Webb |
Correspondent | J.d. Webb RENOVIS SURGICAL TECHNOLOGIES, LLC 1001 OAKWOOD BLVD Round Rock, TX 78681 |
Product Code | MNI |
Subsequent Product Code | KWP |
Subsequent Product Code | MNH |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-06-15 |
Decision Date | 2010-12-07 |
Summary: | summary |