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

LORENZ EXTERNAL MANDIBULAR DISTRACTOR

K Number: K992873 · Decision Sep 17, 1999
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
59
Applicant Total
56
Review Days
22

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Basic Information

Device Name
LORENZ EXTERNAL MANDIBULAR DISTRACTOR
K Number
K992873
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
872.4760
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Walter Lorenz Surgical, Inc.
Date Received
August 26, 1999
Decision Date
September 17, 1999
Product Code
MQN
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
MQN External Mandibular Fixator And/Or Distractor

Similar 510(k) Clearances

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

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Other Clearances by Walter Lorenz Surgical, Inc.

K Number Device Name
K063386 LORENZ ORTHODONTIC ANCHORAGE SYSTEM
K063052 LORENZ TITANIUM FRACTURE / RECONSTRUCTION DEVICES AND PRE-BENT PLATES
K063506 LORENZ STERNAL CLOSURE SYSTEM
K062842 TWIST DRILL
K061384 LORENZ PECTUS SUPPORT BAR, TITANIUM; LORENZ PECTUS SUPPORT BAR STABILIZER, TITANIUM
K042516 OTOMIMIX
K030425 LORENZ RESORBABLE DISTRACTION SYSTEM OR EXPANDER
K040990 MODIFICATION TO SELF-DRILLING RADIOGRAPHIC MARKERS
K040983 LORENZ SELF-DRILLING IMF SCREW
K033740 LORENZ STERNAL CLOSURE SYSTEM
Search all 56 clearances from Walter Lorenz Surgical, Inc. →