The following data is part of a premarket notification filed by Medicrea Technologies with the FDA for Pass Lp Spinal System.
| Device ID | K082577 |
| 510k Number | K082577 |
| Device Name: | PASS LP SPINAL SYSTEM |
| Classification | Orthosis, Spondylolisthesis Spinal Fixation |
| Applicant | MEDICREA TECHNOLOGIES 1001 OAKWOOD BLVD Round Rock, TX 78681 |
| Contact | J D Webb |
| Correspondent | J D Webb MEDICREA TECHNOLOGIES 1001 OAKWOOD BLVD Round Rock, TX 78681 |
| Product Code | MNH |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-09-05 |
| Decision Date | 2008-10-03 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 03613720234760 | K082577 | 000 |