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HARRIER-SA Lumbar Interbody System

FDA UDI

Class II (US FDA UDI)

by Choicespine, LP

Identity

Trade Name
HARRIER-SA Lumbar Interbody System FDA UDI
Generic Name
Surgical mallet FDA UDI
Device Name
HARRIER-SA,MALLET FDA UDI
Model / Reference
Y070-0036 FDA UDI
Description
HARRIER-SA,MALLET FDA UDI

Identifiers

Primary DI / UDI-DI
00840996174565 FDA UDI
510(k) Number
K180519 FDA UDI
FDA Product Code
OVD FDA UDI
MAX FDA UDI
GMDN Term
Surgical mallet FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3080 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical mallet

HARRIER-SA Lumbar Interbody System by Choicespine, LP — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical mallet.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Choicespine, LP

Sources (1)

  • FDA UDI 678b558b-5aec-48e5-97a4-2670ea1bf7c4 35 fields · synced Jun 8, 2026