The following data is part of a premarket notification filed by Stryker Instruments with the FDA for Stryker Silverglide Bipolar Forceps Reusable Cable; Disposable Cable.
| Device ID | K061835 |
| 510k Number | K061835 |
| Device Name: | STRYKER SILVERGLIDE BIPOLAR FORCEPS REUSABLE CABLE; DISPOSABLE CABLE |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | STRYKER INSTRUMENTS 4100 EAST MILHAM AVE. Kalamazoo, MI 49001 |
| Contact | Jean W Sheppard |
| Correspondent | Jean W Sheppard STRYKER INSTRUMENTS 4100 EAST MILHAM AVE. Kalamazoo, MI 49001 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-06-29 |
| Decision Date | 2006-09-08 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 34546540532061 | K061835 | 000 |
| 04546540532053 | K061835 | 000 |