The following data is part of a premarket notification filed by Karl Storz Endoscopy-america, Inc. with the FDA for Ksea Flipptack.
| Device ID | K982571 |
| 510k Number | K982571 |
| Device Name: | KSEA FLIPPTACK |
| Classification | Fastener, Fixation, Nondegradable, Soft Tissue |
| Applicant | KARL STORZ ENDOSCOPY-AMERICA, INC. 600 CORPORATE POINTE Culver City, CA 90230 -7600 |
| Contact | Kevin Kennan |
| Correspondent | Kevin Kennan KARL STORZ ENDOSCOPY-AMERICA, INC. 600 CORPORATE POINTE Culver City, CA 90230 -7600 |
| Product Code | MBI |
| Subsequent Product Code | GED |
| Subsequent Product Code | HRX |
| CFR Regulation Number | 888.3040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-07-24 |
| Decision Date | 1998-09-22 |
| Summary: | summary |