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

MITEK MICRO ANCHOR

K Number: K982420 · Decision Aug 24, 1998
Classifications
1
FEI Numbers
245
Registration Numbers
245
Same Product Code
230
Applicant Total
30
Review Days
70

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Basic Information

Device Name
MITEK MICRO ANCHOR
K Number
K982420
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mitek Products
Date Received
June 15, 1998
Decision Date
August 24, 1998
Product Code
JDR
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
JDR Staple, Fixation, Bone

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JDR), ordered by most recent decision date.

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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 →