FZPClass II
Clip, Implantable
21 CFR 878.4300 / General, Plastic Surgery
FZP is the FDA product code for Clip, Implantable, a class II device type, regulated under 21 CFR 878.4300. As of , FDA records hold 177 510(k) clearances under this code, the most recent dated , and 45 recalls.
Classification record
- Product code
- FZP
- Device name
- Clip, Implantable
- Regulation
- 21 CFR 878.4300
- Device class
- Class II
- Review panel
- General, Plastic Surgery
- Submission type
- 510(k)
- Implant
- Yes
- Life sustaining or supporting
- No
- GMP exempt
- No
- Third party review eligible
- No
- Ingested clearances
- 178
- Ingested recalls
- 45
Clearances, product code FZP
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 1977 | 2 |
| 1980 | 2 |
| 1981 | 2 |
| 1982 | 1 |
| 1983 | 2 |
| 1984 | 7 |
| 1985 | 3 |
| 1986 | 5 |
| 1987 | 1 |
| 1988 | 1 |
| 1990 | 3 |
| 1991 | 1 |
| 1992 | 3 |
| 1993 | 3 |
| 1994 | 3 |
| 1995 | 4 |
| 1996 | 4 |
| 1997 | 4 |
| 1998 | 7 |
| 1999 | 5 |
| 2000 | 4 |
| 2001 | 7 |
| 2002 | 5 |
| 2003 | 10 |
| 2004 | 7 |
| 2005 | 6 |
| 2006 | 7 |
| 2007 | 6 |
| 2008 | 4 |
| 2009 | 3 |
| 2010 | 6 |
| 2011 | 3 |
| 2012 | 2 |
| 2013 | 3 |
| 2014 | 3 |
| 2015 | 8 |
| 2016 | 5 |
| 2017 | 4 |
| 2018 | 4 |
| 2019 | 1 |
| 2020 | 2 |
| 2022 | 3 |
| 2023 | 3 |
| 2024 | 2 |
| 2025 | 5 |
| 2026 | 2 |
Applicants with the most clearances
Product code FZP| Applicant | Clearances |
|---|---|
| United States Surgical, A Division of Tyco Healthc | 17 |
| AtriCure, Inc. | 11 |
| Ethicon, Inc | 11 |
| Cardica, Inc. | 10 |
| Coalescent Surgical | 7 |
| Medtronic, Inc. | 7 |
| Edward Weck, Inc. | 7 |
| Teleflex Medical | 7 |
| Niti Medical Technologies, Ltd. | 5 |
| Taiwan Surgical Corporation | 5 |
Companies listing this code with FDA
Companies whose registered establishments list this codeFIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.