The following data is part of a premarket notification filed by Spinal Usa with the FDA for S-lok Pss System.
Device ID | K122931 |
510k Number | K122931 |
Device Name: | S-LOK PSS SYSTEM |
Classification | Orthosis, Spinal Pedicle Fixation |
Applicant | SPINAL USA 1001 OAKWOOD BLVD Round Rock, TX 78681 |
Contact | J.d. Webb |
Correspondent | J.d. Webb SPINAL USA 1001 OAKWOOD BLVD Round Rock, TX 78681 |
Product Code | MNI |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-09-24 |
Decision Date | 2012-11-20 |
Summary: | summary |