FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

IMBIBE NEEDLE

K Number: K140414 · Decision Apr 1, 2014
Classifications
1
FEI Numbers
1140
Registration Numbers
1140
Same Product Code
57
Applicant Total
22
Review Days
42

Basic Information

Device Name
IMBIBE NEEDLE
K Number
K140414
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.4540
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ORTHOVITA, INC.
Date Received
February 18, 2014
Decision Date
April 1, 2014
Product Code
LXH
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
LXH Orthopedic Manual Surgical Instrument

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