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Specials

FDA UDI

Class II (US FDA UDI)

by SeaSpine Orthopedics Corporation

Identity

Trade Name
Specials FDA UDI
Generic Name
Orthopaedic implant driver FDA UDI
Device Name
Modified Bullet Nose Saddle Driver FDA UDI
Model / Reference
SR-0693 FDA UDI
Description
Modified Bullet Nose Saddle Driver FDA UDI

Identifiers

Catalog Number
SR-0693 FDA UDI
Primary DI / UDI-DI
10889981277789 FDA UDI
510(k) Number
K180176 FDA UDI
FDA Product Code
NKB FDA UDI
GMDN Term
Orthopaedic implant driver FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 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: Orthopaedic implant driver

Specials by SeaSpine Orthopedics Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implant driver.

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 b206b38d-3545-4631-ae2a-f129de031b2e 36 fields · synced Jun 8, 2026