← Back to catalogue

Guide Pin 2.7 x 100mm w Olive

FDA UDI

Class I (US FDA UDI)

by OsteoCentric Technologies, Inc

Identity

Trade Name
Guide Pin 2.7 x 100mm w Olive FDA UDI
Generic Name
Surgical drill guide obturator FDA UDI
Device Name
Guide Pin 2.7 x 100mm Olive FDA UDI
Model / Reference
317-0001 FDA UDI
Description
Guide Pin 2.7 x 100mm Olive FDA UDI

Identifiers

Catalog Number
317-0001 FDA UDI
Primary DI / UDI-DI
00816950029325 FDA UDI
510(k) Number
K210247 FDA UDI
FDA Product Code
FZX FDA UDI
GMDN Term
Surgical drill guide obturator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Dimensions & Sizes

Size
Guidewire Diameter — 2.7 Millimeter FDA UDI
Guidewire Length — 100 Millimeter FDA UDI

Category: Surgical drill guide obturator

Guide Pin 2.7 x 100mm w Olive by OsteoCentric Technologies, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical drill guide obturator.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 11166b59-645d-408c-85be-204ea17db399 37 fields · synced Jun 8, 2026