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

OSTEOMED ALVEOLAR DISTRACTION SYSTEM

K Number: K030790 · Decision Sep 10, 2003
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
59
Applicant Total
29
Review Days
182

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Basic Information

Device Name
OSTEOMED ALVEOLAR DISTRACTION SYSTEM
K Number
K030790
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4760
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Osteomed LP
Date Received
March 12, 2003
Decision Date
September 10, 2003
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

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Other Clearances by Osteomed LP

K Number Device Name
K143338 Argulated Locking Plates
K133691 EXTRIMILOCK ANKLE PLATING SYSTEM
K131445 OSTEOMED EXTREMILOCK FOOT PLATING SYSTEM
K123885 OSTEOMED SMARTFLEX CRANIAL SPRING DISTRACTOR
K123207 PRIMALIF TM LLIF UNITARY PEEK LATERAL LUMBAR INTERBODY FUSION SYSTEM
K120015 OSTEOMED WRIST PLATING SYSTEM
K111419 OSTEOMED HAND FUSION SYSTEM
K111176 OSTEOMED LOW PROFILE NEURO FIXATION SYSTEM
K102438 PRIMALOK FACET FIXATION SYSTEM
K100354 PRIMAL OK INTERSPINOUS FUSION SYSTEM
Search all 29 clearances from Osteomed LP →