The following data is part of a premarket notification filed by Orthosoft, Inc. with the FDA for Navitrack System Total Hip Replacement,model 900.200.
| Device ID | K022364 |
| 510k Number | K022364 |
| Device Name: | NAVITRACK SYSTEM TOTAL HIP REPLACEMENT,MODEL 900.200 |
| Classification | Neurological Stereotaxic Instrument |
| Applicant | ORTHOSOFT, INC. 75 QUEEN ST., SUITE 3300 Montreal, Quebec, CA H3c 2n6 |
| Contact | Christopher Mclean |
| Correspondent | Christopher Mclean ORTHOSOFT, INC. 75 QUEEN ST., SUITE 3300 Montreal, Quebec, CA H3c 2n6 |
| Product Code | HAW |
| CFR Regulation Number | 882.4560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-07-22 |
| Decision Date | 2003-02-04 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00889024492677 | K022364 | 000 |
| 00889024492660 | K022364 | 000 |