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ZipFix

FDA UDI

Class II (US FDA UDI)

by Synthes

Identity

Trade Name
ZipFix FDA UDI
Generic Name
Sternal fixation device FDA UDI
Device Name
STERNAL ZIPFIX WITH NEEDLE STERILE/20 PACK FDA UDI
Model / Reference
08.501.001.20S FDA UDI
Description
STERNAL ZIPFIX WITH NEEDLE STERILE/20 PACK FDA UDI

Identifiers

Catalog Number
0850100120S FDA UDI
Primary DI / UDI-DI
20887587025992 FDA UDI
510(k) Number
K110789 FDA UDI
FDA Product Code
JDQ FDA UDI
GMDN Term
Sternal fixation device FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3010 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Sternal fixation device

ZipFix by Synthes — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sternal fixation device.

Cleared under the same submission

K110789 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Synthes

Sources (1)

  • FDA UDI ce354f09-d24b-406b-9078-323c2c1a5446 36 fields · synced May 30, 2026