The following data is part of a premarket notification filed by Interpore Intl. with the FDA for Porous Hydroxyapatite Bg200.
| Device ID | K841201 |
| 510k Number | K841201 |
| Device Name: | POROUS HYDROXYAPATITE BG200 |
| Classification | Bone Grafting Material, Synthetic |
| Applicant | INTERPORE INTL. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | LYC |
| CFR Regulation Number | 872.3930 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-03-21 |
| Decision Date | 1984-08-03 |