FDA.reportPublic FDA data

BULLET-TIP PEEK IBF SYSTEM

Primary DI
00846468034528
Brand
BULLET-TIP PEEK IBF SYSTEM
Company
Pioneer Surgical Technology, Inc.
Model
32-CTAMP
Catalog number
32-CTAMP
Device description
CORNER TAMP
Published
2019-12-21
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
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
HXGTAMP

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HXGTampOrthopedic1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00846468015732PrimaryGS10
00846468034528PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00846468015732008464680157328464680157320846468015732
00846468034528008464680345288464680345280846468034528

GMDN Terms#

Term, Definition table
TermDefinition
General internal orthopaedic fixation system implantation kitA collection of instruments and devices intended to be used for the placement of an internal orthopaedic fixation system into or onto all types of bones (e.g., bones of limbs, spine, pelvis, or craniomaxillofacial). It is a non-dedicated device that includes various metallic and/or plastic reusable devices [e.g., retractors, rods, clamps, drills, pins, saws, screwdrivers, guides, trials, impactors] intended to be used for the implantation of any type of internal orthopaedic fixation system; the implant(s) is not included. This is a reusable device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+1(386)418-8888labeling@rtix.com
+1(906)226-9909labeling@resolvesurg.com
+1(906)226-9909regulatory@exalta.com

Regulatory Flags#

DUNS number
793384496
Device count
1
DM exempt
false
Premarket exempt
true
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

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00840298701902CODA™ Anterior Cervical Plate System58-2022010102022-01-0102023-01-19
00840298701971CODA™ Anterior Cervical Plate System58-2022010242022-01-0242023-01-19
00840298702039CODA™ Anterior Cervical Plate System58-2022020282022-02-0282023-01-19
00840298702268CODA™ Anterior Cervical Plate System58-2022040802022-04-0802023-01-19
00840298700134CODA™ Anterior Cervical Plate System58-202221018S2022-21-018S2023-01-19
00840298700028CODA™ Anterior Cervical Plate System58-202220014S2022-20-014S2023-01-19
00840298700110CODA™ Anterior Cervical Plate System58-202221014S2022-21-014S2023-01-19
00840298700677CODA™ Anterior Cervical Plate System58-2022302002022-30-2002023-01-24
00840298701957CODA™ Anterior Cervical Plate System58-2022010202022-01-0202023-01-19
00840298702022CODA™ Anterior Cervical Plate System58-2022020262022-02-0262023-01-19
00840298702251CODA™ Anterior Cervical Plate System58-2022040762022-04-0762023-01-19
00840298700608CODA™ Anterior Cervical Plate System58-2022222002022-22-2002023-01-24
00840298700776CODA™ Anterior Cervical Plate System58-2022100072022-10-0072023-01-25
00840298700905CODA™ Anterior Cervical Plate System58-2022207172022-20-7172023-01-19
00840298701933CODA™ Anterior Cervical Plate System58-2022010162022-01-0162023-01-19
00840298701988CODA™ Anterior Cervical Plate System58-2022010262022-01-0262023-01-19
00840298702091CODA™ Anterior Cervical Plate System58-2022020402022-02-0402023-01-19
00840298702114CODA™ Anterior Cervical Plate System58-2022020442022-02-0442023-01-19
00840298702138CODA™ Anterior Cervical Plate System58-2022030452022-03-0452023-01-19
00840298702176CODA™ Anterior Cervical Plate System58-2022030572022-03-0572023-01-19

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00190776416423MillenniumAvalign Technologies, Inc.HXG2026-02-16
00190776416430MillenniumAvalign Technologies, Inc.HXG2026-02-16
00190376538990Intervertebral Disc Preparation InstrumentsALPHATEC SPINE, INC.HXG2026-02-10
00190376694351IdentiTiALPHATEC SPINE, INC.HXG2026-02-10
00190376694368Intervertebral Disc Preparation InstrumentsALPHATEC SPINE, INC.HXG2026-02-10
00190376700700IdentiTiALPHATEC SPINE, INC.HXG2026-02-10
00190376700717IdentiTiALPHATEC SPINE, INC.HXG2026-02-10
00810112598902TriLeap Lower Extremity Anatomic Plating SystemCROSSROADS EXTREMITY SYSTEMSHXG2026-02-10
00190776415723MillenniumAvalign Technologies, Inc.HXG2026-02-04
04026575341153Endo-Model Knee Fusion Nail SK InstrumentsWALDEMAR LINK GmbH & Co. KGHXG2026-02-02
00840180543429General InstrumentsALPHATEC SPINE, INC.HXG2025-12-31
00840180543597General InstrumentsALPHATEC SPINE, INC.HXG2025-12-31
00840180543757General InstrumentsALPHATEC SPINE, INC.HXG2025-12-31
03662663155625Zyston Interbody Spacer SystemHighridge Medical, LLCHXG2025-12-29
03662663156707Zyston Interbody Spacer SystemHighridge Medical, LLCHXG2025-12-29
10889981285999FacetSeaspine Orthopedics CorporationHXG2025-12-19
03662663242233Alta ACDF SystemHighridge Medical, LLCHXG2025-12-18
03662663242240Alta ACDF SystemHighridge Medical, LLCHXG2025-12-18
03662663160674Zyston Interbody Spacer SystemHighridge Medical, LLCHXG2025-12-16
03662663160681Zyston Interbody Spacer SystemHighridge Medical, LLCHXG2025-12-16
03662663160698Zyston Interbody Spacer SystemHighridge Medical, LLCHXG2025-12-16
03662663246620Alta ACDF SystemHighridge Medical, LLCHXG2025-12-16
03662663254113Alta ACDF SystemHighridge Medical, LLCHXG2025-12-16
03662663254120Alta ACDF SystemHighridge Medical, LLCHXG2025-12-16
00190376662176IdentiTi IIALPHATEC SPINE, INC.HXG2025-12-08
00199150041930Medtronic Reusable InstrumentsMEDTRONIC SOFAMOR DANEK, INC.HXG2025-11-20
03662663070942TMT InstrumentsHighridge Medical, LLCHXG2025-11-16
03662663071581TMT InstrumentsHighridge Medical, LLCHXG2025-11-16
00888480363101C-THRU Anterior Spinal Spacer SystemHighridge Medical, LLCHXG2025-11-14
00888480637370Breckenridge ACDF SystemHighridge Medical, LLCHXG2025-11-14