FDA.reportPublic FDA data

COALESCE

Primary DI
B1422000000910000
Brand
COALESCE
Company
VERTERA, INC.
Model
2000-00-091000
Device description
9x23x10MM COALESCE-Straight, Parallel
Published
2017-11-09
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
MAXIntervertebral Fusion Device With Bone Graft, Lumbar

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
MAXIntervertebral Fusion Device With Bone Graft, LumbarOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K143685000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K143685000Hedgehog Cervical Interbody Fusion DeviceVertera, Inc.2015-09-23ODP

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
B1422000000910000PrimaryHIBCC0

GMDN Terms#

Term, Definition table
TermDefinition
Polymeric spinal fusion cage, sterileA sterile device intended to help fuse segments of the spine to treat anatomical abnormalities of the vertebrae, typically due to degenerative intervertebral disks [i.e., degenerative disc disease (DDD)]. The device is typically designed as a small, hollow and/or porous, threaded or fenestrated cylinder (or other geometric form) and is made of non-bioabsorbable synthetic polymer [e.g., polyetheretherketone (PEEK)] that is implanted between the bones or bone grafts of the spine, to provide mechanical stability and sufficient space for bone fusion to occur. Disposable devices associated with implantation may be included.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
078812764
Device count
1
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
B14211000000010Cohere1100-00-00012018-11-09
B14211000000140Cohere1100-00-00142018-11-09
B14211000000160Cohere1100-00-00162018-11-09
B14211000100010Cohere1100-01-00012018-11-09
B1422000001012080COALESCE2000-00-1012082018-11-09
B1422000001014080COALESCE2000-00-1014082018-11-09
B14220000128080COALESCE2000-01-28082018-11-09
B14220000128090COALESCE2000-01-28092018-11-09
B14220000128100COALESCE2000-01-28102018-11-09
B14220000128110COALESCE2000-01-28112018-11-09
B14220000128120COALESCE2000-01-28122018-11-09
B14220000128140COALESCE2000-01-28142018-11-09
B14220000132090COALESCE2000-01-32092018-11-09
B14220000132100COALESCE2000-01-32102018-11-09
B14220000132110COALESCE2000-01-32112018-11-09
B14220000132120COALESCE2000-01-32122018-11-09
B14220000132140COALESCE2000-01-32142018-11-09
B14220000132160COALESCE2000-01-32162018-11-09
B1422000000908000COALESCE2000-00-0908002017-11-09
B1422000000908080COALESCE2000-00-0908082017-11-09

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00197157075859ZAVATION INSERTERZavation LLCMAX2026-05-27
00810166522366X-PACEXPANDING INNOVATIONS, INC.MAX2026-05-27
00810166522373X-PACEXPANDING INNOVATIONS, INC.MAX2026-05-27
B70712535005S0Dual X Graft Tamp ShortAMPLIFY SURGICAL, INC.MAX2026-05-27
B707129410010130DUALXS T/PLIF 15 DEG x 9-12MMAMPLIFY SURGICAL, INC.MAX2026-05-27
B707129410010200DUALXS T/PLIF 18 DEG x 10-13MMAMPLIFY SURGICAL, INC.MAX2026-05-27
07613153046196AVS PLStryker CorporationMAX2015-09-14
07613153046202AVS PLStryker CorporationMAX2015-09-14
07613153046219AVS PLStryker CorporationMAX2015-09-14
07613153046233AVS PLStryker CorporationMAX2015-09-14
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