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

ADJUSTABLE BONE PLATES BIOABSORBABLE, SELF COMPRESSION BONE FIXATION SYSTEM & ACCESSORIES

K Number: K072528 · Decision Dec 28, 2007
Classifications
1
FEI Numbers
106
Registration Numbers
106
Same Product Code
291
Applicant Total
16
Review Days
112

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Basic Information

Device Name
ADJUSTABLE BONE PLATES BIOABSORBABLE, SELF COMPRESSION BONE FIXATION SYSTEM & ACCESSORIES
K Number
K072528
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4760
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Prosurg, Inc.
Date Received
September 7, 2007
Decision Date
December 28, 2007
Product Code
JEY
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
JEY Plate, Bone

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Other Clearances by Prosurg, Inc.

K Number Device Name
K152511 Neo - Arthroscope (Rigid) 2.0mm/3.5mm, Outer sheath/ cannula, Outer sheath/ cannula w/ Handle, Trocar for outersheath/ cannula
K152466 Neo-Bronchoscope -Digital Video Bronchoscopy System(Rigid/Flexible)
K152619 Neoscope 3D - 3D Digital Video Endoscopic System (Rigid/Flexible)
K120766 ENDOSCOPIC DIAGNOSTIC & TREATMENT SYSTEM (MODIFICATION)
K071138 CRANIOCLAMP BIOABSORBABLE CRANIAL BONE FLAP FIXATION SYSTEM
K070737 XSORB BIOABSORBABLE CRANIOFACIAL BONE FIXATION SYSTEM & ACCESSORIES
K070846 MINISLING ADJUSTABLE POLYMER SLING & SURGICAL MESH WITH SELF-ANCHORING SYSTEM
K060326 LASERTX - DIODE LASER & DELIVERY SYSTEM
K050488 TURBT-RF ELECTRODES AND ELECTROSURGICAL DEVICES
K042780 NEOSCOPE - ENDOSCOPIC DIAGNOSTIC & TREATMENT SYSTEM
Search all 16 clearances from Prosurg, Inc. →