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FORWARD CUTTING MONOBLOC REAMER, HUDSON, Ø7.5mm

FDA UDI

Class II (US FDA UDI)

by Advanced Orthopaedic Solutions, Inc.

Identity

Trade Name
FORWARD CUTTING MONOBLOC REAMER, HUDSON, Ø7.5mm FDA UDI
Generic Name
Medullary canal orthopaedic reamer, flexible FDA UDI
Model / Reference
0251-075 FDA UDI

Identifiers

Primary DI / UDI-DI
00848665001174 FDA UDI
510(k) Number
K021008 FDA UDI
K070444 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Medullary canal orthopaedic reamer, flexible FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Medullary canal orthopaedic reamer, flexible

FORWARD CUTTING MONOBLOC REAMER, HUDSON, Ø7.5mm by Advanced Orthopaedic Solutions, Inc. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Medullary canal orthopaedic reamer, flexible.

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 cbf5f555-5b89-4652-9890-602c0ec24278 34 fields · synced Jun 8, 2026