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

BIOSTOP G BONE CEMENT RESTRICTOR

K Number: K943727 · Decision May 11, 1995
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
36
Applicant Total
15
Review Days
282

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Basic Information

Device Name
BIOSTOP G BONE CEMENT RESTRICTOR
K Number
K943727
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.3300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Landos, Inc.
Date Received
August 2, 1994
Decision Date
May 11, 1995
Product Code
LZN
Advisory Committee
General, Plastic Surgery
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
LZN Cement Obturator

Similar 510(k) Clearances

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

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Other Clearances by Landos, Inc.

K Number Device Name
K964226 MEMORY STAPLE (20 SIZES AVAILABLE)
K971069 TWIST-OFF (TM) SCREW
K971070 SCARF THREAD-HEAD (TM) HEAD SCREW
K971068 34MM SCARF THREAD-HEAD(TM) SCREW
K961732 KAR
K970846 22.2/+4MM CO CR & ZIRCONIA FEMORAL HEAD
K953111 CORAIL
K962233 TWIST-OFF SCREW
K962236 SCARF THREAD-HEAD SCREW
K960642 NANCY NAIL
Search all 15 clearances from Landos, Inc. →