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

FIXATION (STEINMANN) PINS

K Number: K013888 · Decision May 1, 2002
Classifications
1
FEI Numbers
283
Registration Numbers
283
Same Product Code
203
Applicant Total
23
Review Days
159

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Basic Information

Device Name
FIXATION (STEINMANN) PINS
K Number
K013888
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Miltex, Inc.
Date Received
November 23, 2001
Decision Date
May 1, 2002
Product Code
HTY
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
HTY Pin, Fixation, Smooth

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K072563 MILTEX RIGID CONTAINER SYSTEMS
K061033 MILTEX RIGID STERILIZATION CONTAINER SYSTEM, (47 COMPONENTS)
K052018 MILTEX LIGATING CLIP
K050570 MILTEX RIGID STERILIZATION CONTAINER SYSTEM
K043013 MILTEX LAPAROSCOPIC INSTRUMENTS
K954185 RE-BAG MULTI-USE POUCH, LARGE & SMALL
K823324 DENTAL INSTRUMENTS - PROBES
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