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

RESOLVE QUICKANCHOR

K Number: K993575 · Decision Dec 29, 1999
Classifications
1
FEI Numbers
71
Registration Numbers
71
Same Product Code
79
Applicant Total
30
Review Days
69

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Basic Information

Device Name
RESOLVE QUICKANCHOR
K Number
K993575
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4880
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mitek Products
Date Received
October 21, 1999
Decision Date
December 29, 1999
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 Mitek Products

K Number Device Name
K013572 MITEK BIOCRYL INTERFERENCE SCREWS
K013781 RIDIDFIX 2.7MM BTB CROSS PIN KIT
K002639 BIOKNOTLESS ANCHOR
K010633 RIGIDFIX SOFT TISSUE ACL CROSSPIN SYSTEM
K002406 MITEK 2GII MENISCAL REPAIR SYSTEM
K003076 MITEK CUFFTACK
K002402 VAPR TC ELECTRODE FOR USE WITH VAPR II ELECTROSURGICAL SYSTEM
K002422 VARPR 3.5MM 90 SUCTION ELECTRODE FOR USE WITH VAPR SYSTEM
K000936 VAPR 2.3MM WEDGE ELECTRODE FOR USE WITH VAPR SYSTEM
K993327 TALON ANCHOR SNAP-PAK
Search all 30 clearances from Mitek Products →