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FDA 510(k), K943540, SURGICAL CUTTING BURS
FDA 510(k), K943540, SURGICAL CUTTING BURS
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510(K) Number: K943540
Device Name: SURGICAL CUTTING BURS
Manufacturer: STRYKER CORP.
Device Classification Name: Driver, Wire, And Bone Drill, Manual
Regulation Number: 872.4120
Classification Product Code: DZJ
Date Received: 07/22/1994
Decision Date: 11/30/1994
Regulation Medical Specialty: Dental
Device Name: SURGICAL CUTTING BURS
Manufacturer: STRYKER CORP.
Device Classification Name: Driver, Wire, And Bone Drill, Manual
Regulation Number: 872.4120
Classification Product Code: DZJ
Date Received: 07/22/1994
Decision Date: 11/30/1994
Regulation Medical Specialty: Dental
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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