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

BONE PLATE

K Number: K931244 · Decision Feb 15, 1994
Classifications
1
FEI Numbers
519
Registration Numbers
519
Same Product Code
1313
Applicant Total
43
Review Days
341

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Basic Information

Device Name
BONE PLATE
K Number
K931244
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
March 11, 1993
Decision Date
February 15, 1994
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

Similar 510(k) Clearances

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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. →