The following data is part of a premarket notification filed by Medicrea International with the FDA for Pass Lp Spinal System.
Device ID | K112493 |
510k Number | K112493 |
Device Name: | PASS LP SPINAL SYSTEM |
Classification | Orthosis, Spinal Pedicle Fixation |
Applicant | MEDICREA INTERNATIONAL 1001 OAKWOOD BLVD Round Rock, TX 78681 |
Contact | J.d. Webb |
Correspondent | J.d. Webb MEDICREA INTERNATIONAL 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 | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-08-29 |
Decision Date | 2011-11-21 |
Summary: | summary |