FDA.report

IdentiTi II

Primary DI
00190376694375
Brand
IdentiTi II
Company
ALPHATEC SPINE, INC.
Model
801-200
Device description
ID II LIF INSERTER
Published
2026-02-18
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
false

Related Records

Product Codes

CodeName
PHMIntervertebral fusion device with bone graft, thoracic

Product Code Classifications

CodeDeviceSpecialtyClass
PHMIntervertebral Fusion Device With Bone Graft, ThoracicOrthopedic2

Premarket Submissions

SubmissionSupplement
K242364000

Premarket Details

SubmissionSupplementDeviceApplicantDecision dateProduct code
K242364000IdentiTi™ II Interbody SystemAlphatec Spine, Inc.2024-10-04MAX

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
00190376694375PrimaryGS10

GMDN Terms

TermDefinition
Orthopaedic inorganic implant inserter/extractor, reusableA hand-held manual surgical instrument designed for the surgical insertion and/or extraction of a non-tissue based (inorganic) orthopaedic implant (e.g., a bone nail, spiral blade, or bone fixation plate). It is an instrument in a one-piece or modular configuration with a region that will attach/fit/lock to part of the implant, and typically features either a mechanism to apply a striking force (e.g., on a pad/flange) a mechanism for twisting (screwing) (e.g., T-handle), or a plunger mechanism to deploy a guide to drive the implant into place. This is a reusable device.

Sterilization Methods

Method
Moist Heat or Steam Sterilization

Contacts

PhoneEmail
+1(760)431-9286Regulatory@alphatecspine.com

Regulatory Flags

DUNS number
602465783
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
true

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Primary DIBrandCompanyProduct codePublished
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00190376722016IdentiTi IIALPHATEC SPINE, INC.PHM2026-02-18
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