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Sternalock 360 System

FDA UDI

Class II (US FDA UDI)

by Biomet Microfixation, Inc

Identity

Trade Name
STERNALOCK 360 SYSTEM FDA UDI
Generic Name
Bone-coring punch, reusable FDA UDI
Model / Reference
74-1193 FDA UDI

Identifiers

Catalog Number
74-1193 FDA UDI
Primary DI / UDI-DI
00841036275273 FDA UDI
510(k) Number
K151019 FDA UDI
K161896 FDA UDI
FDA Product Code
HRS FDA UDI
GMDN Term
Bone-coring punch, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 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: Bone-coring punch, reusable

Sternalock 360 System by Biomet Microfixation, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone-coring punch, reusable.

Cleared under the same submission

K151019 also covers:

K161896 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biomet Microfixation, Inc

Sources (1)

  • FDA UDI e47ac1c4-14c2-4fac-a46b-d167643cb3ad 35 fields · synced May 31, 2026