K102081 is an FDA 510(k) clearance for the ENDOSCOPIC CLIP SYSTEM. This device is classified as a Clip, Implantable (Class II - Special Controls, product code FZP).
Submitted by Aesculap, Inc. (Center Valley, US). The FDA issued a Cleared decision on August 6, 2010, 11 days after receiving the submission on July 26, 2010.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4300.
| 510(k) Number | K102081 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 26, 2010 |
| Decision Date | August 06, 2010 |
| Days to Decision | 11 days |
| Submission Type | Special |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | FZP — Clip, Implantable |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 878.4300 |