The following data is part of a premarket notification filed by Coligne, Ag with the FDA for Ostapek Interbody Fusion Cages.
| Device ID | K181963 |
| 510k Number | K181963 |
| Device Name: | OstaPek Interbody Fusion Cages |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | coLigne, AG Utoquai 43 Zurich, CH Ch 8008 |
| Contact | Robert Lange |
| Correspondent | J. D. Webb The OrthoMedix Group, Inc. 1001 Oakwood Blvd Round Rock, TX 78681 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-07-23 |
| Decision Date | 2018-11-14 |
| Summary: | summary |