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FDA 510(k), K951904, SYNTHES (USA) [SYNTHES] POINT CONTACT FIXATOR PLATE [PC-FIX]
FDA 510(k), K951904, SYNTHES (USA) [SYNTHES] POINT CONTACT FIXATOR PLATE [PC-FIX]
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510(K) Number: K951904
Device Name: SYNTHES (USA) [SYNTHES] POINT CONTACT FIXATOR PLATE [PC-FIX]
Manufacturer: ANGELA J SILVESTRI
Device Classification Name: Device, Fixation, Proximal Femoral, Implant
Regulation Number: JDO
Classification Product Code: 04/24/1995
Date Received: 07/17/1995
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic
Device Name: SYNTHES (USA) [SYNTHES] POINT CONTACT FIXATOR PLATE [PC-FIX]
Manufacturer: ANGELA J SILVESTRI
Device Classification Name: Device, Fixation, Proximal Femoral, Implant
Regulation Number: JDO
Classification Product Code: 04/24/1995
Date Received: 07/17/1995
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic
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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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