Biomet® OrthoPak® Non-invasive Bone Growth Stimulator System; Biomet® SpinalPak® Non-invasive Spine Fusion Stimulator Sy
Device Facts
| Record ID | P850022 |
|---|---|
| Device Name | Biomet® OrthoPak® Non-invasive Bone Growth Stimulator System; Biomet® SpinalPak® Non-invasive Spine Fusion Stimulator Sy |
| Applicant | Ahp Eos Buyer, Inc. |
| Product Code | LOF · Orthopedic |
| Decision Date | Feb 18, 1986 |
| Decision | APPR |
| Regulation | 21 CFR 890.5870 |
| Device Class | Class 2 |
