510(k) K113598
K113598 is an FDA 510(k) premarket notification submitted by Stryker Medical for the device "POWER-LOAD COT FASTENER SYSTEM". The FDA issued a decision of Substantially Equivalent on December 20, 2011. The device falls under product code FPO (Stretcher, Wheeled), a Class II device regulated under 21 CFR 880.6910. Stryker Medical has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 20, 2011
- Date Received
- December 5, 2011
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- Yes
Device Classification
- Device Name
- Stretcher, Wheeled
- Device Class
- Class II
- Regulation Number
- 880.6910
- Review Panel
- HO
- Submission Type