FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

SPINAL MICROKNIFE

K Number: K882525 · Decision Sep 22, 1988
Classifications
1
FEI Numbers
117
Registration Numbers
117
Same Product Code
8
Applicant Total
17
Review Days
97

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Basic Information

Device Name
SPINAL MICROKNIFE
K Number
K882525
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.4540
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Karlin Technology, Inc.
Date Received
June 17, 1988
Decision Date
September 22, 1988
Product Code
HTS
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
HTS Knife, Orthopedic

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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
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. →