FDA.report

MD Vue Lateral Access

Primary DI
00840019918992
Brand
MD Vue Lateral Access
Company
PRECISION SPINE, INC.
Model
54-BR-0080
Catalog number
54-BR-0080
Device description
80mm Right Blade
Published
2019-03-28
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
false

Related Records

Product Codes

CodeName
GADRetractor

Product Code Classifications

CodeDeviceSpecialtyClass
GADRetractorGeneral, Plastic Surgery1

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
00840019918992PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifierGTIN-14 normalizedUPC-AEAN-13
00840019918992008400199189928400199189920840019918992

GMDN Terms

TermDefinition
Neurosurgical retraction system, spinalA frame-like assembly of surgical instruments/devices intended to be used to create a self-locking, self-retaining mechanism dedicated to the temporary parting of dorsal tissue to enable access for spinal surgery. It includes a mounting frame, with retracting blades which may come together to form a tube-like port; it may be intended to attach to a fixed arm, e.g., an arm attached to the surgical table. This is a reusable device.

Sterilization Methods

Method
Moist Heat or Steam Sterilization

Regulatory Flags

DUNS number
079398589
Device count
1
DM exempt
true
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
false
Serial number
false
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
true

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