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 |