FDA.report

ATEC Posterior Navigation Disc Prep Instruments

Primary DI
00190376529295
Brand
ATEC Posterior Navigation Disc Prep Instruments
Company
ALPHATEC SPINE, INC.
Model
244-03-000-14-N
Device description
POST NAV ROTATING DISTRACTOR, 14mm
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
00190376529295PrimaryGS10

GMDN Terms

TermDefinition
Bone lever/elevator, reusableA manual surgical instrument designed to lift, position, or pry up (elevate) bone, other anatomical structures, or surgical material/devices during an orthopaedic intervention. It is made of high-grade stainless steel and is available in a wide variety of sizes, designs, and blade shapes. It is typically a robust instrument with a blunted blade with no cutting edge at the distal end that can be pointed, rounded, flat, curved or hook shaped and a handle of various designs at the proximal end. Some types can have special functions, e.g., for angle joint operations or for luxation procedures. This is a reusable device.

Device Sizes

TypeValueUnit
Width14Millimeter

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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