ES2 Neuromonitoring Accessory Instruments— 510(k) K171807
Substantially EquivalentStryker Corporation
FDA 510(k) clearance K171807 for ES2 Neuromonitoring Accessory Instruments, Substantially Equivalent on 2017-07-18. Applicant: Stryker Corporation. Device class: 2.
Clearance details
- Applicant
- Stryker Corporation
- Product code
- Code PDQ
- Device class
- Class 2
- Regulation
- 21 CFR 874.1820
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Allendale, NJ, US
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