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Intergro Dbm

by Biomet Spine LLC

510(k) K082793

Intergro Dbm is a Class II device made by Biomet Spine LLC, cleared under FDA 510(k) K082793 on 2 Apr 2009, 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 NumberK082793 Date2 Apr 2009ClearedStatusActive

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  • Withdrawn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
FDA applicant
Biomet Spine
Device class
Class II
Regulation
21 CFR Part 888.3045
Advisory committee
Orthopedic
FDA decision
SESE Substantially Equivalent

Related clearances

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

Cited by

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

Devices cleared under K082793

16 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 K082793
UDI-DISize and differences
InterGro DBM Paste DBM001
Biomet Orthopedics, Inc.
DBM001 / DBM00100888480585121 —On the market
InterGro DBM Paste DBM002
Biomet Orthopedics, Inc.
DBM002 / DBM00200888480585138 —On the market
InterGro DBM Paste DBM005
Biomet Orthopedics, Inc.
DBM005 / DBM00500888480585145 —On the market
InterGro DBM Plus DBMW02
Biomet Orthopedics, Inc.
DBMW02 / DBMW0200888480585213 —On the market
InterGro DBM Plus DBMW05
Biomet Orthopedics, Inc.
DBMW05 / DBMW0500888480585220 —On the market
InterGro DBM Plus DBMW10
Biomet Orthopedics, Inc.
DBMW10 / DBMW1000888480585251 —On the market
InterGro DBM Putty DBM010
Biomet Orthopedics, Inc.
DBM010 / DBM01000888480585169 —On the market
StaGraft DBM Paste 92-2022
Biomet Orthopedics, Inc.
92-2022 / 92-202200880304706408 —On the market
StaGraft DBM Plus 92-2005
Biomet Orthopedics, Inc.
92-2005 / 92-200500880304684874 —On the market
StaGraft DBM Plus 92-2006
Biomet Orthopedics, Inc.
92-2006 / 92-200600880304683907 —On the market
StaGraft DBM Plus 92-2007
Biomet Orthopedics, Inc.
92-2007 / 92-200700880304684881 —On the market
StaGraft DBM Putty 92-2000
Biomet Orthopedics, Inc.
92-2000 / 92-200000880304684836 —On the market
StaGraft DBM Putty 92-2001
Biomet Orthopedics, Inc.
92-2001 / 92-200100880304686816 —On the market
StaGraft DBM Putty 92-2002
Biomet Orthopedics, Inc.
92-2002 / 92-200200880304684850 —On the market
StaGraft DBM Putty 92-2003
Biomet Orthopedics, Inc.
92-2003 / 92-200300880304686830 —On the market
StaGraft DBM Putty 92-2004
Biomet Orthopedics, Inc.
92-2004 / 92-200400880304684867 —On the market

Similar devices

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

Other devices from Biomet Spine LLC

See all devices from Biomet Spine LLC →