The following data is part of a premarket notification filed by Stryker Gmbh with the FDA for Adapt For Gamma3.
| Device ID | K173946 |
| 510k Number | K173946 |
| Device Name: | ADAPT For Gamma3 |
| Classification | Orthopedic Stereotaxic Instrument |
| Applicant | Stryker GmbH Bohnackerweg 1 Selzach, CH 2545 |
| Contact | Nesli Karakaya |
| Correspondent | Nesli Karakaya Stryker GmbH Bohnackerweg 1 Selzach, CH 2545 |
| Product Code | OLO |
| CFR Regulation Number | 882.4560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-12-27 |
| Decision Date | 2018-05-02 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 07613327311822 | K173946 | 000 |
| 07613327298192 | K173946 | 000 |