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TS-Bone Hip Plate

FDA UDI

Class II (US FDA UDI)

by Orthopedic Sciences, Inc

Identity

Trade Name
TS-Bone Hip Plate FDA UDI
Generic Name
Orthopaedic bone screw, non-bioabsorbable, sterile FDA UDI
Device Name
30mm TS-Bone Titanium Compression Screw FDA UDI
Model / Reference
PST-030 FDA UDI
Description
30mm TS-Bone Titanium Compression Screw FDA UDI

Identifiers

Catalog Number
PST-030 FDA UDI
Primary DI / UDI-DI
00813892020052 FDA UDI
510(k) Number
K063709 FDA UDI
FDA Product Code
HRS FDA UDI
GMDN Term
Orthopaedic bone screw, non-bioabsorbable, sterile 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Dimensions & Sizes

Size
Length — 30 Millimeter FDA UDI

Category: Orthopaedic bone screw, non-bioabsorbable, sterile

TS-Bone Hip Plate by Orthopedic Sciences, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone screw, non-bioabsorbable, sterile.

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 f50d2eaf-4659-43c0-9466-ea8c1269b1e9 38 fields · synced May 30, 2026