FDA.report

ATEC Posterior Navigation Disc Prep Instruments

Primary DI
00190376528854
Brand
ATEC Posterior Navigation Disc Prep Instruments
Company
ALPHATEC SPINE, INC.
Model
244-05-11092210-N
Device description
POST NAV PS Trial 11 x 9 x 22mm, 10°
Published
2024-04-20
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
OLOOrthopedic stereotaxic instrument

Product Code Classifications

CodeDeviceSpecialtyClass
OLOOrthopedic Stereotaxic InstrumentNeurology2

Premarket Submissions

SubmissionSupplement
K232345000

Premarket Details

SubmissionSupplementDeviceApplicantDecision dateProduct code
K232345000ATEC Posterior Navigated Disc Prep InstrumentsAlphatec Spine, Inc.2023-11-02OLO

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
00190376528854PrimaryGS10

GMDN Terms

TermDefinition
Spinal implant trialA copy of a final spinal prosthesis, graft, or other implantable spinal device (e.g., may include intervertebral disc prosthesis, spinal cage, spinal hook) used to validate the proper size of the permanent implant required by the patient, to determine its appropriate position, and/or to verify that the implant site has been cut to the proper dimensions. It can be made of metal or plastic. This is a reusable device.

Device Sizes

TypeValueUnit
Angle10degree
Height11Millimeter
Length22Millimeter
Width9Millimeter

Sterilization Methods

Method
Moist Heat or Steam Sterilization

Contacts

PhoneEmail
+1(760)431-9286Regulatory@alphatecspine.com

Regulatory Flags

DUNS number
602465783
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
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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