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

COBB SPINAL ELEVATORS

K Number: K882068 · Decision Jun 3, 1988
Classifications
1
FEI Numbers
321
Registration Numbers
321
Same Product Code
429
Applicant Total
17
Review Days
17

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Basic Information

Device Name
COBB SPINAL ELEVATORS
K Number
K882068
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3050
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Karlin Technology, Inc.
Date Received
May 17, 1988
Decision Date
June 3, 1988
Product Code
KWP
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
KWP Appliance, Fixation, Spinal Interlaminal

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Other Clearances by Karlin Technology, Inc.

K Number Device Name
K903969 SUCTION RETRACTOR(TOWER ATTACH.)FOR CRANK FRAM RET
K893201 BONE PLATE
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
Search all 17 clearances from Karlin Technology, Inc. →