The following data is part of a premarket notification filed by New Era Orthopaedics, Llc with the FDA for New Era Orthopaedics Polyscrew Pedicle Screw System.
Device ID | K141253 |
510k Number | K141253 |
Device Name: | NEW ERA ORTHOPAEDICS POLYSCREW PEDICLE SCREW SYSTEM |
Classification | Orthosis, Spinal Pedicle Fixation |
Applicant | NEW ERA ORTHOPAEDICS, LLC 1001 OAKWOOD BLVD. Round Rock, TX 78681 |
Contact | J.d. Webb |
Correspondent | J.d. Webb NEW ERA ORTHOPAEDICS, LLC 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 | 2014-05-14 |
Decision Date | 2015-01-09 |
Summary: | summary |