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

SPINAL SURGERY FRAME

K Number: K882078 · Decision Jun 16, 1988
Classifications
1
FEI Numbers
162
Registration Numbers
162
Same Product Code
60
Applicant Total
17
Review Days
30

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Basic Information

Device Name
SPINAL SURGERY FRAME
K Number
K882078
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4950
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Karlin Technology, Inc.
Date Received
May 17, 1988
Decision Date
June 16, 1988
Product Code
FWZ
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FWZ Operating Room Accessories Table Tray

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FWZ), ordered by most recent decision date.

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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. →