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VV-Plug 667145-751

by Oscor Inc.

VV-Plug 667145-751 is a Class II device made by Oscor Inc., cleared under FDA 510(k) K031164 on 19 Jun 2003 and listed in FDA GUDID since 15 Nov 2017 (UDI-DI 00885672008307), active as of 22 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 22 Oct 2026

Documents

510(k) K031164

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00885672008307 UDI-DI Date15 Nov 2017ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)ST from GUDID Special NumberK031164 Date19 Jun 2003DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K031164 decided 19 Jun 2003 Active
  • FDA GUDID UDI-DI 00885672008307 listed 15 Nov 2017 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K031164
  2. Listed FDA GUDID 00885672008307

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name
VV-Plug
Generic name
Implantable pulse generator port plug
Model / Ref / Catalog
667145-751, VV-PLUG
Primary DI / UDI-DI
00885672008307
510(k) Number
FDA product code
DTD
GMDN term
Implantable pulse generator port plug
Device class
Class II
Regulation number
870.3620
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 3.2 Millimeter

Similar devices in this category

Other devices filed under Implantable pulse generator port plug.

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Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)