FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

NEXA CARPO METACARPAL IMPLANT

K Number: K060386 · Decision May 10, 2006
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
25
Applicant Total
16
Review Days
85

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Basic Information

Device Name
NEXA CARPO METACARPAL IMPLANT
K Number
K060386
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3770
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nexa Orthopedics, Inc.
Date Received
February 14, 2006
Decision Date
May 10, 2006
Product Code
KYI
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KYI Prosthesis, Wrist, Carpal Trapezium

Similar 510(k) Clearances

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Other Clearances by Nexa Orthopedics, Inc.

K Number Device Name
K072710 NEXFIX COMPRESSION PIN
K071147 NEXA ORTHOPEDICS TOTAL SHOULDER SYSTEM
K070688 NEXFIX COMPRESSION STAPLE
K060071 NEXA COMPRESSION SCREW
K053408 NEXA BONE PLATE AND SCREW SYSTEM
K053394 NEXA BONE SCREW SYSTEM
K051740 TAPERED COMPRESSION PIN
K051406 OSTEOCURE RESORBABLE BEAD KIT
K033046 SUBTALAR PEG IMPLANT
K032902 SUBTALAR ARTHRORISIS IMPLANT
Search all 16 clearances from Nexa Orthopedics, Inc. →