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FDA 510(k) K023562, MODIFICATION TO CLASSIC GREAT TOE IMPLANT, by Nexa Orthopedics, Inc.

FDA 510(k) K023562, MODIFICATION TO CLASSIC GREAT TOE IMPLANT, by Nexa Orthopedics, Inc.

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510(K) Number: K023562
Device Name: MODIFICATION TO CLASSIC GREAT TOE IMPLANT
Manufacturer: Nexa Orthopedics, Inc.
Device Classification Name: prosthesis, toe, constrained, polymer
Regulation Number: 888.3720
Classification Product Code: KWH
Date Received: 10/23/2002
Decision Date: 11/13/2002
Regulation Medical Specialty: Orthopedic
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