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MBlock Adjustable Loop BTB

by S.B.M

MBlock Adjustable Loop BTB (05.05.0117) is a Class II device made by S.B.M, cleared under FDA 510(k) K202193 on 16 Oct 2020 and listed in FDA GUDID since 16 Nov 2020 (UDI-DI 03760304680304), 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

510(k) K202193

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number03760304680304 UDI-DI Date16 Nov 2020ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Special NumberK202193 Date16 Oct 2020DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K202193 decided 16 Oct 2020 Active
  • FDA GUDID UDI-DI 03760304680304 listed 16 Nov 2020 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K202193
  2. Listed FDA GUDID 03760304680304

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
MBlock
Generic name
Tendon/ligament bone anchor, non-bioabsorbable
Model / Ref / Catalog
Adjustable Loop BTB, 05.05.0117
Primary DI / UDI-DI
03760304680304
510(k) Number
FDA product code
MBI
GMDN term
Tendon/ligament bone anchor, non-bioabsorbable
Device class
Class II
Regulation number
888.3040
GUDID distribution status
In Commercial Distribution

Similar devices in this category

Other devices filed under Tendon/ligament bone anchor, non-bioabsorbable.

Other devices from S.B.M

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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)