FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

MITEK DRILL GUIDE

K Number: K892904 · Decision Sep 28, 1989
Classifications
1
FEI Numbers
92
Registration Numbers
92
Same Product Code
6
Applicant Total
31
Review Days
161

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Basic Information

Device Name
MITEK DRILL GUIDE
K Number
K892904
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.4540
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Mitek Surgical Products, Inc.
Date Received
April 20, 1989
Decision Date
September 28, 1989
Product Code
HXY
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
HXY Brace, Drill

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Other Clearances by Mitek Surgical Products, Inc.

K Number Device Name
K953560 MITEK THREADED ANCHOR (FASTIN)
K953877 MITEK GII ANCHOR
K936311 MITEK MINI ANCHOR
K941599 MITEK ABSORBABLE ANCHOR
K944051 ABSORBALBE ANCHOR
K950070 MITEK TOGGLE ANCHOR(TM)
K944936 MITEK G III ANCHOR, MITEK LS ANCHOR
K945203 MITEK THRADED ANCHOR (MTA)
K934366 MITEK CANCELLOUS FIXATION SCREW, CORTICAL FIXATION SCREW, SOFT TISSUE WASHER
K931782 MITEK GIII ANCHOR
Search all 31 clearances from Mitek Surgical Products, Inc. →