The following data is part of a premarket notification filed by Encore Orthopedics, Inc. with the FDA for Cemstop Cement Restrictor.
| Device ID | K993841 |
| 510k Number | K993841 |
| Device Name: | CEMSTOP CEMENT RESTRICTOR |
| Classification | Cement Obturator |
| Applicant | ENCORE ORTHOPEDICS, INC. 9800 METRIC BLVD. Austin, TX 78758 |
| Contact | Debbie De Los Santos |
| Correspondent | Debbie De Los Santos ENCORE ORTHOPEDICS, INC. 9800 METRIC BLVD. Austin, TX 78758 |
| Product Code | LZN |
| CFR Regulation Number | 878.3300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-11-12 |
| Decision Date | 2000-05-04 |
| Summary: | summary |