The following data is part of a premarket notification filed by Orthopedic Systems, Inc. with the FDA for Corin Modular Moore Stem.
| Device ID | K881288 |
| 510k Number | K881288 |
| Device Name: | CORIN MODULAR MOORE STEM |
| Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Uncemented |
| Applicant | ORTHOPEDIC SYSTEMS, INC. 1897 NATIONAL AVE. Hayward, CA 94545 |
| Contact | Robert R Moore |
| Correspondent | Robert R Moore ORTHOPEDIC SYSTEMS, INC. 1897 NATIONAL AVE. Hayward, CA 94545 |
| Product Code | LWJ |
| CFR Regulation Number | 888.3360 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-03-28 |
| Decision Date | 1988-06-29 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 05055196927896 | K881288 | 000 |
| 05055196927889 | K881288 | 000 |