STRYKER ARIA PNEUMATIC SYSTEM
FDA 510(k) clearance K061725 · decided 2006-10-26
Clearance details
- K-number
- K061725
- Device name
- STRYKER ARIA PNEUMATIC SYSTEM
- Applicant
- Stryker Instruments
- Decision
- Substantially Equivalent
- Date received
- 2006-06-19
- Decision date
- 2006-10-26
- Days to decision
- 129 days
- Clearance type
- Traditional
- Product code
- HBB
- Device class
- 2
- Regulation number
- 882.4370
- Medical specialty
- Neurology
- Advisory committee
- Neurology
- Location
- Kalamazoo, MI, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.