The following data is part of a premarket notification filed by Ostex Intl., Inc. with the FDA for Osteomark.
| Device ID | K961562 |
| 510k Number | K961562 |
| Device Name: | OSTEOMARK |
| Classification | Column Chromatography & Color Development, Hydroxyproline |
| Applicant | OSTEX INTL., INC. 2203 AIRPORT WAY SOUTH SUITE 400 Seattle, WA 98134 |
| Contact | Nancy Mallinak |
| Correspondent | Nancy Mallinak OSTEX INTL., INC. 2203 AIRPORT WAY SOUTH SUITE 400 Seattle, WA 98134 |
| Product Code | JMM |
| CFR Regulation Number | 862.1400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-04-22 |
| Decision Date | 1996-07-11 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() OSTEOMARK 74801494 1819369 Live/Registered |
ALERE NORTH AMERICA, LLC 1990-09-24 |
![]() OSTEOMARK 74099485 1819553 Live/Registered |
ALERE NORTH AMERICA, LLC 1990-09-24 |