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 |