The following data is part of a premarket notification filed by Porex Medical with the FDA for Medpar Surgical Implants.
| Device ID | K832283 |
| 510k Number | K832283 |
| Device Name: | MEDPAR SURGICAL IMPLANTS |
| Classification | Prosthesis, Chin, Internal |
| Applicant | POREX MEDICAL 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | FWP |
| CFR Regulation Number | 878.3550 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-07-12 |
| Decision Date | 1984-05-10 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 07613252170297 | K832283 | 000 |
| 07613252083498 | K832283 | 000 |
| 07613252083481 | K832283 | 000 |
| 07613252083474 | K832283 | 000 |
| 07613252083467 | K832283 | 000 |
| 07613252083429 | K832283 | 000 |
| 07613252083412 | K832283 | 000 |
| 07613252083405 | K832283 | 000 |
| 07613252083399 | K832283 | 000 |
| 07613252083382 | K832283 | 000 |
| 07613252083375 | K832283 | 000 |
| 07613252083504 | K832283 | 000 |
| 07613252083511 | K832283 | 000 |
| 07613252088523 | K832283 | 000 |
| 07613252088516 | K832283 | 000 |
| 07613252088424 | K832283 | 000 |
| 07613252083863 | K832283 | 000 |
| 07613252083856 | K832283 | 000 |
| 07613252083849 | K832283 | 000 |
| 07613252083832 | K832283 | 000 |
| 07613252083825 | K832283 | 000 |
| 07613252083634 | K832283 | 000 |
| 07613252083627 | K832283 | 000 |
| 07613252083368 | K832283 | 000 |