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Allofuse Plus

by Allosource, Inc.

510(k) K103036

Allofuse Plus is a Class II device made by Allosource, Inc., cleared under FDA 510(k) K103036 on 10 Jan 2011, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK103036 Date10 Jan 2011ClearedStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
MQV
Device class
Class II
Regulation
21 CFR Part 888.3045
Advisory committee
Orthopedic
FDA decision
SESE Substantially Equivalent

Related clearances

cited in the FDA summary

Clearances this device's FDA summary refers to, and clearances whose summaries refer to it: a citation, not a claim of equivalence.

Cites

Source: 510k-lineage (choiben314), CC BY 4.0

Devices cleared under K103036

17 devices · FDA GUDID

Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.

Devices cleared under K103036
UDI-DISize and differences
Propel 5020205
NuVasive, LLC
502020500887517970435
Prescription: yes
On the market
Propel 5020205994
NuVasive, LLC
502020599400887517970442
Prescription: yes
On the market
Propel 5020210
NuVasive, LLC
502021000887517970459
Prescription: yes
On the market
Propel 5020210994
NuVasive, LLC
502021099400887517970466
Prescription: yes
On the market
Propel 5020301994
NuVasive, LLC
502030199400887517970480
Prescription: yes
On the market
Propel 5020305994
NuVasive, LLC
502030599400887517971500
Prescription: yes
On the market
Propel 5020310994
NuVasive, LLC
502031099400887517971524
Prescription: yes
On the market
Propel 5020401
NuVasive, LLC
502040100887517971531
Prescription: yes
On the market
Propel 5020401994
NuVasive, LLC
502040199400887517971548
Prescription: yes
On the market
Propel 5020403
NuVasive, LLC
502040300887517971555
Prescription: yes
On the market
Propel 5020403994
NuVasive, LLC
502040399400887517971562
Prescription: yes
On the market
Propel 5020408
NuVasive, LLC
502040800887517971579
Prescription: yes
On the market
Propel 5020408994
NuVasive, LLC
502040899400887517971586
Prescription: yes
On the market
XEMPLIFI 8103.0201S
GLOBUS MEDICAL, INC.
8103.0201S00889095205893
Total Volume 1 mL
Prescription: no
On the market
XEMPLIFI 8103.0203S
GLOBUS MEDICAL, INC.
8103.0203S00889095205909
Total Volume 3 mL
Prescription: no
On the market
XEMPLIFI 8103.0208S
GLOBUS MEDICAL, INC.
8103.0208S00889095205916
Total Volume 8 mL
Prescription: no
On the market
XEMPLIFI 8103.0210S
GLOBUS MEDICAL, INC.
8103.0210S00889095205923
Total Volume 10 mL
Prescription: no
On the market

Similar devices

Other devices filed under FDA product code MQV (Filler, Bone Void, Calcium Compound).

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