Mayfield® 41A1436

by Integra Lifesciences Corp.

Mayfield® 41A1436 is a Class II device made by Integra Lifesciences Corp., cleared under FDA 510(k) K072208 on 7 Sep 2007 (3 earlier submissions) and listed in FDA GUDID since 26 Jul 2016 (UDI-DI 10381780254249), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

+3 more

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number10381780254249 UDI-DI	Date26 Jul 2016Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Special	NumberK072208	Date7 Sep 2007Decided	StatusActive
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK941558	Date6 Dec 1995Decided	StatusActive
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK932860	Date28 Sep 1993Decided	StatusActive
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK923789	Date12 Feb 1993Decided	StatusActive

Official records

AccessGUDID record UDI-DI 10381780254249
FDA 510(k) database 510(k) number K072208
FDA 510(k) database 510(k) number K941558
FDA 510(k) database 510(k) number K932860
FDA 510(k) database 510(k) number K923789

Across registries

2 registries list this device

FDA 510(k) K072208 decided 7 Sep 2007 Active· +3 more in the status table
FDA GUDID UDI-DI 10381780254249 listed 26 Jul 2016 Listed

Timeline

5 dated events

12 Feb 1993 Cleared FDA 510(k) K923789
28 Sep 1993 Cleared FDA 510(k) K932860
6 Dec 1995 Cleared FDA 510(k) K941558
7 Sep 2007 Cleared FDA 510(k) K072208
26 Jul 2016 Listed FDA GUDID 10381780254249

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: Mayfield®
Generic name: Skull clamp
Model / reference: 41A1436

Primary DI / UDI-DI: 10381780254249
510(k) Number: K072208
K923789
K932860
K941558
FDA product code: HBL
GMDN term: Skull clamp

Device class: Class II
Regulation number: 882.4460
GUDID distribution status: In Commercial Distribution

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Properties

Prescription use
Lot / batch number

Other properties (13, all answered No)