The following data is part of a premarket notification filed by Implantech Associates, Inc. with the FDA for Chin Wafer.
| Device ID | K921581 |
| 510k Number | K921581 |
| Device Name: | CHIN WAFER |
| Classification | Prosthesis, Chin, Internal |
| Applicant | IMPLANTECH ASSOCIATES, INC. 1730 PENNSYLVANIA AVENUE, NW Washington, DC 20006 |
| Contact | Joan E Hankin |
| Correspondent | Joan E Hankin IMPLANTECH ASSOCIATES, INC. 1730 PENNSYLVANIA AVENUE, NW Washington, DC 20006 |
| Product Code | FWP |
| CFR Regulation Number | 878.3550 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-04-02 |
| Decision Date | 1992-05-06 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| M724GLM21 | K921581 | 000 |
| M724GLE21 | K921581 | 000 |