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Sinefix

FDA UDI

Class II (US FDA UDI)

by Baat Medical Products B.V.

Identity

Trade Name
SINEFIX FDA UDI
Generic Name
Tendon/ligament bone anchor, non-bioabsorbable FDA UDI
Device Name
Lateral Driver FDA UDI
Model / Reference
Lateral Driver FDA UDI
Description
Lateral Driver FDA UDI

Identifiers

Catalog Number
60004 FDA UDI
Primary DI / UDI-DI
08720629959191 FDA UDI
510(k) Number
K220966 FDA UDI
FDA Product Code
MBI FDA UDI
GMDN Term
Tendon/ligament bone anchor, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Tendon/ligament bone anchor, non-bioabsorbable

Sinefix by Baat Medical Products B.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tendon/ligament bone anchor, non-bioabsorbable.

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 466bcb48-f099-421d-affc-5fc2ace4732d 35 fields · synced Jun 8, 2026