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

BONE PLATE

K Number: K893201 · Decision Apr 4, 1990
Classifications
1
FEI Numbers
519
Registration Numbers
519
Same Product Code
1313
Applicant Total
17
Review Days
343

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Basic Information

Device Name
BONE PLATE
K Number
K893201
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Karlin Technology, Inc.
Date Received
April 26, 1989
Decision Date
April 4, 1990
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 Karlin Technology, Inc.

K Number Device Name
K903969 SUCTION RETRACTOR(TOWER ATTACH.)FOR CRANK FRAM RET
K893203 BONE SCREW
K882525 SPINAL MICROKNIFE
K882519 X-RAY MARKER
K882520 SHOULDER BOLSTER, KNEE, ANKLE & LEG SUPPORT PADS
K882073 SPINAL NEEDLE
K882524 UNIVERSALLY ADJUSTABLE ARMBOARD
K882069 SPINAL DISTRACTORS, SPANNERS
K882072 ORTHOPAEDIC AND SPINAL RING CURRETTES
K882077 MICRODISCECTOMY CURRETTES
Search all 17 clearances from Karlin Technology, Inc. →