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

MITEK MINI QUICKANCHOR PLUS

K Number: K992487 · Decision Sep 21, 1999
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
30
Review Days
57

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Basic Information

Device Name
MITEK MINI QUICKANCHOR PLUS
K Number
K992487
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mitek Products
Date Received
July 26, 1999
Decision Date
September 21, 1999
Product Code
HWC
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
HWC Screw, Fixation, Bone

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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
K993575 RESOLVE QUICKANCHOR
Search all 30 clearances from Mitek Products →