The following data is part of a premarket notification filed by Endius, Inc. with the FDA for Endius Atavi System.
| Device ID | K053267 |
| 510k Number | K053267 |
| Device Name: | ENDIUS ATAVI SYSTEM |
| Classification | Arthroscope |
| Applicant | ENDIUS, INC. 23 WEST BACON ST. Plainville, MA 02762 |
| Contact | Christine Kuntz-nassif |
| Correspondent | Christine Kuntz-nassif ENDIUS, INC. 23 WEST BACON ST. Plainville, MA 02762 |
| Product Code | HRX |
| CFR Regulation Number | 888.1100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2005-11-23 |
| Decision Date | 2006-01-13 |
| Summary: | summary |