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

MILTEX MEMBRANE TACK KIT

K Number: K092855 · Decision Dec 29, 2009
Classifications
1
FEI Numbers
71
Registration Numbers
71
Same Product Code
79
Applicant Total
23
Review Days
104

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Basic Information

Device Name
MILTEX MEMBRANE TACK KIT
K Number
K092855
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4880
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Miltex, Inc.
Date Received
September 16, 2009
Decision Date
December 29, 2009
Product Code
DZL
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
DZL Screw, Fixation, Intraosseous

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Other Clearances by Miltex, Inc.

K Number Device Name
K101653 MILTEX THOMPSON CASSETTES; MILTEX SURGICAL CASSETTES
K083796 MILTEX ASPIRATING SYRINGE, MILTEX PETITE ASPIRATING SYRINGE, MILTEX SELF-ASPIRATING SYRINGE, MILTEX LIGHTWEIGHT
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
K013888 FIXATION (STEINMANN) PINS
K954185 RE-BAG MULTI-USE POUCH, LARGE & SMALL
K823324 DENTAL INSTRUMENTS - PROBES
Search all 23 clearances from Miltex, Inc. →