The following data is part of a premarket notification filed by Howmedica Corp. with the FDA for Alta Tibial/upper Extremity Metaphyseal Plate Sys.
| Device ID | K885250 |
| 510k Number | K885250 |
| Device Name: | ALTA TIBIAL/UPPER EXTREMITY METAPHYSEAL PLATE SYS |
| Classification | Plate, Fixation, Bone |
| Applicant | HOWMEDICA CORP. 359 VETERANS BLVD. Rutherford, NJ 07070 |
| Contact | Robert E Smith |
| Correspondent | Robert E Smith HOWMEDICA CORP. 359 VETERANS BLVD. Rutherford, NJ 07070 |
| Product Code | HRS |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-12-22 |
| Decision Date | 1989-02-13 |