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 |