The following data is part of a premarket notification filed by Barry Markman, M.d. with the FDA for Markman Template System.
| Device ID | K970306 |
| 510k Number | K970306 |
| Device Name: | MARKMAN TEMPLATE SYSTEM |
| Classification | Stylet, Surgical, General & Plastic Surgery |
| Applicant | BARRY MARKMAN, M.D. 3085 EAST FLAMINGO, SUITE A Las Vegas, NV 89121 |
| Contact | Barry S Markman, M.d. |
| Correspondent | Barry S Markman, M.d. BARRY MARKMAN, M.D. 3085 EAST FLAMINGO, SUITE A Las Vegas, NV 89121 |
| Product Code | GAH |
| CFR Regulation Number | 878.4800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-01-27 |
| Decision Date | 1997-11-20 |