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

ORTHOPAEDIC WIRES

K Number: K942603 · Decision Nov 9, 1994
Classifications
1
FEI Numbers
41
Registration Numbers
41
Same Product Code
7
Applicant Total
43
Review Days
161

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Basic Information

Device Name
ORTHOPAEDIC WIRES
K Number
K942603
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Acu Med, Inc.
Date Received
June 1, 1994
Decision Date
November 9, 1994
Product Code
LRN
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
LRN Wire, Surgical

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Other Clearances by Acu Med, Inc.

K Number Device Name
K021321 WRIST FUSION PLATE
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
Search all 43 clearances from Acu Med, Inc. →