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G7 Osseoti Acetabular Shell

FDA UDI

Class II (US FDA UDI)

by Biomet Orthopedics, Inc.

Identity

Trade Name
G7 OSSEOTI ACETABULAR SHELL FDA UDI
Generic Name
Acetabular shell FDA UDI
Model / Reference
110010260 FDA UDI

Identifiers

Catalog Number
110010260 FDA UDI
Primary DI / UDI-DI
00880304544352 FDA UDI
510(k) Number
K140669 FDA UDI
FDA Product Code
KWZ FDA UDI
PBI FDA UDI
OQH FDA UDI
OQG FDA UDI
JDI FDA UDI
LZO FDA UDI
OQI FDA UDI
LPH FDA UDI
GMDN Term
Acetabular shell FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3310 FDA UDI
888.3350 FDA UDI
888.3358 FDA UDI
888.3353 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Acetabular shell

G7 Osseoti Acetabular Shell by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Acetabular shell.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 36e5e6ae-879b-490d-a6f8-49717906dc34 36 fields · synced May 31, 2026