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

ASCENSION TOTAL PLATE SYSTEM

K Number: K100502 · Decision Aug 2, 2010
Classifications
1
FEI Numbers
519
Registration Numbers
519
Same Product Code
1313
Applicant Total
22
Review Days
161

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Basic Information

Device Name
ASCENSION TOTAL PLATE SYSTEM
K Number
K100502
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ascension Orthopedics, Inc.
Date Received
February 22, 2010
Decision Date
August 2, 2010
Product Code
HRS
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
HRS Plate, Fixation, Bone

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Other Clearances by Ascension Orthopedics, Inc.

K Number Device Name
K233674 Freedom Wrist Arthroplasty System
K233670 Ascension Silicone MCP; Ascension Silicone PIP
K121826 INTEGRA PROXIMAL HUMERAL PLATE SYSTEM
K110700 ASCENSION ATLAS HUMERAL PLATING SYSTEM
K102549 THE ASCENSION MOVEMENT GREAT TOE SYSTEM TOTAL ARTHROPLASTY
K100448 ASCENSION MODULAR TOTAL SHOULDER SYSTEM
K100925 ASCENSION ANKLE FUSION NAIL SYSTEM
K100176 ASCENSION ANKLE FUSION PLATE SYSTEM
K092047 ASCENSION METAL GREAT TOE SYSTEM
K092440 ASCENSION CANNULATED SCREW SYSTEM
Search all 22 clearances from Ascension Orthopedics, Inc. →