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Invisx™

FDA UDI

Class II (US FDA UDI)

by Medtronic PS Medical

Identity

Trade Name
INVISX™ FDA UDI
Generic Name
Cranial bone flap fixation clip FDA UDI
Device Name
LOCK 60110 INVISX SHELF PK 10 X 2 PK FDA UDI
Model / Reference
60110 FDA UDI
Description
LOCK 60110 INVISX SHELF PK 10 X 2 PK FDA UDI

Identifiers

Primary DI / UDI-DI
00613994845023 FDA UDI
510(k) Number
K010361 FDA UDI
FDA Product Code
GXN FDA UDI
GMDN Term
Cranial bone flap fixation clip FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5330 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Width — 2.54 Millimeter FDA UDI

Category: Cranial bone flap fixation clip

Invisx™ by Medtronic PS Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cranial bone flap fixation clip.

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 3d804c5b-cf05-47b6-b5a4-bfa6025fecfb 36 fields · synced May 31, 2026