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

NEXFIX COMPRESSION STAPLE

K Number: K070688 · Decision May 18, 2007
Classifications
1
FEI Numbers
245
Registration Numbers
245
Same Product Code
230
Applicant Total
16
Review Days
67

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Basic Information

Device Name
NEXFIX COMPRESSION STAPLE
K Number
K070688
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nexa Orthopedics, Inc.
Date Received
March 12, 2007
Decision Date
May 18, 2007
Product Code
JDR
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
JDR Staple, Fixation, Bone

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
K060386 NEXA CARPO METACARPAL IMPLANT
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. →