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

WRIST FUSION PLATE

K Number: K021321 · Decision Jul 17, 2002
Classifications
1
FEI Numbers
519
Registration Numbers
519
Same Product Code
1313
Applicant Total
43
Review Days
83

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Basic Information

Device Name
WRIST FUSION PLATE
K Number
K021321
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Acu Med, Inc.
Date Received
April 25, 2002
Decision Date
July 17, 2002
Product Code
HRS
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
HRS Plate, Fixation, Bone

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Other Clearances by Acu Med, Inc.

K Number Device Name
K013616 POLARUS CAP SCREW
K012655 CONGRUENT BONE PLATE SYSTEM
K992525 ACUMED MODULAR SHOULDER SYSTEM
K993657 ACUMED SUTURE ANCHOR
K980103 ACUMED SUTURE ANCHOR
K965028 ACUMED SUTURE WASHER
K965029 STABLELOC II EXTERNAL FIXATOR
K964500 ACUMED TENSION BAND PIN
K963026 TBD
K963118 EXTREMITY BONE SCREW
Search all 43 clearances from Acu Med, Inc. →