ShefaBone SCPC Resorbable Bone Graft

K153230 · The Implantech Inc./Shefabone · LYC · Jul 14, 2016 · Dental

Device Facts

Record IDK153230
Device NameShefaBone SCPC Resorbable Bone Graft
ApplicantThe Implantech Inc./Shefabone
Product CodeLYC · Dental
Decision DateJul 14, 2016
DecisionSESE
Submission TypeTraditional
Regulation21 CFR 872.3930
Device ClassClass 2
AttributesTherapeutic

Intended Use

ShefaBone SCPC Resorbable Bioactive Bone Graft, is a silica-calcium phosphate composite, synthetic bone graft material for use in oral, dental intraosseous, and maxillofacial bone defects. Typical uses include: - Periodontal / infrabony defects - Ridge augmentation (sinusotomy, osteotomy, cystectomy) - Extraction sites (ridge maintenance/augmentation, implant preparation/ placement) - Sinus lifts - Cystic cavities - Oral and maxillofacial augmentation

Device Story

ShefaBone SCPC is a synthetic, resorbable bioactive bone graft material composed of silica, calcium, phosphate, and sodium. It functions as a bone void filler to support bone regeneration in oral, dental, and maxillofacial defects. The device is supplied as porous particles in a glass vial, sterilized by gamma radiation. It is intended for use by dental professionals in clinical settings. The material is packed into bony voids or gaps to facilitate augmentation or repair. Its porous structure and chemical composition are designed to be resorbed over time while providing a scaffold for new bone growth, aiding in clinical outcomes for procedures like sinus lifts and ridge maintenance.

Clinical Evidence

Bench testing only. No clinical data provided.

Technological Characteristics

Silica-calcium phosphate composite; ionic Si, Ca, P, Na composition; porous structure; particle size 90-710 microns; supplied in 1g (1cc) glass vials; sterilized by gamma radiation.

Indications for Use

Indicated for patients requiring bone grafting in oral, dental intraosseous, and maxillofacial defects, including periodontal/infrabony defects, ridge augmentation, extraction sites, sinus lifts, and cystic cavities.

Regulatory Classification

Identification

Bone grafting material is a material such as hydroxyapatite, tricalcium phosphate, polylactic and polyglycolic acids, or collagen, that is intended to fill, augment, or reconstruct periodontal or bony defects of the oral and maxillofacial region.

Special Controls

*Classification.* (1) Class II (special controls) for bone grafting materials that do not contain a drug that is a therapeutic biologic. The special control is FDA's “Class II Special Controls Guidance Document: Dental Bone Grafting Material Devices.” (See § 872.1(e) for the availability of this guidance document.)(2) Class III (premarket approval) for bone grafting materials that contain a drug that is a therapeutic biologic. Bone grafting materials that contain a drug that is a therapeutic biologic, such as biological response modifiers, require premarket approval. (c) *Date premarket approval application (PMA) or notice of product development protocol (PDP) is required.* Devices described in paragraph (b)(2) of this section shall have an approved PMA or a declared completed PDP in effect before being placed in commercial distribution.

Predicate Devices

Reference Devices

Related Devices

Submission Summary (Full Text)

{0}------------------------------------------------ Image /page/0/Picture/1 description: The image is a black and white logo for the U.S. Department of Health & Human Services. The logo features a stylized image of three human profiles facing to the right, stacked on top of each other. The profiles are connected and appear to be emerging from a single form. The logo is encircled by the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA". Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002 July 14, 2016 Shefabone Incorporated % Elaine Duncan President Paladin Medical, Inc. P.O. Box 560 Stillwater, Minnesota 55082 Re: K153230 Trade/Device Name: ShefaBone SCPC Resorbable Bone Graft Regulation Number: 21 CFR 872.3930 Regulation Name: Bone Grafting Material Regulatory Class: Class II Product Code: LYC Dated: June 7, 2016 Received: June 8, 2016 Dear Elaine Duncan: We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading. If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register. {1}------------------------------------------------ Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting (reporting of medical devicerelated adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (OS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Division of Industry and Consumer Education at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance. You may obtain other general information on your responsibilities under the Act from the Division of Industry and Consumer Education at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm. Sincerely yours, # Michael J. Ryan -S for Erin I. Keith, M.S. Director Division of Anesthesiology, General Hospital, Respiratory, Infection Control, and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ ## Indications for Use 510(k) Number (if known) K153230 Device Name ShefaBone SCPC Resorbable Bone Graft Indications for Use (Describe) Resorbable Bone Graft (Describe) ShefaBone SCPC Resorbable Bioactive Bone Graft, is a silica-calcium phosphate composite, synthetic bone graft material for use in oral, dental intraosseous, and maxillofacial bone defects. Typical uses include: - · Periodontal / infrabony defects - · Ridge augmentation (sinusotomy, osteotomy, cystectomy) - · Extraction sites (ridge maintenance/augmentation, implant preparation/ placement) - Sinus lifts - · Cystic cavities - · Oral and maxillofacial augmentation Type of Use (Select one or both, as applicable) X Prescription Use (Part 21 CFR 801 Subpart D) | Over-The-Counter Use (21 CFR 801 Subpart C) ### PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON A SEPARATE PAGE IF NEEDED. #### FOR FDA USE ONLY Concurrence of Center for Devices and Radiological Health (CDRH) (Signature) {3}------------------------------------------------ This section applies only to requirements of the Paperwork Reduction Act of 1995. #### *DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.* The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to: > Department of Health and Human Services Food and Drug Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff PRAStaff(@fda.hhs.gov "An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number." {4}------------------------------------------------ ## 510(K) SUMMARY ## Submitted on behalf of: Shefabone Incorporated c/o Ahmed El-Ghannam President 9016 Cliff Cameron Drive, Ste 201 Charlotte, NC 28269 à^K Ò|æ ^´Ö´ } & } & É É È È È È È È È È È (CONTACT PERSON) Ú¦¹•ãã^} dÃ√≥ dÃ√ áããã ÁT ^ â ãã có 8 ã UUAOI CAI EA Scal, actif baile G Ï FÍ ÐÏ Í JË €H Á I FI E I JE HI €A Á ÖŒ½ÒÁ½­ÜÒÚŒÏÒÖ½Á Rǐ |ˆ  ʴœFÎ Á A VÜC£ÖÒÍÞŒ ÒK ÔUT T UÞÁŒ Ó½ ÖSCEJURIOS OF OFF OF OK ÙÜÙ ÆÕÙ ÕÕÍÀ V4| @} vK Øger Krister Area Bron ShefaBone SCPC Resorbable Bone Graft Ó[ } ^송[ ãÁã|^! Ó[ } ^Áð¦æðã *Á æð¹ľæÁÁ ŠÝÔÁ A #### DESCRIPTION of the DEVICE: ShefaBone SCPC Áã Áæ¹·ˆ} o@ ããÁ¦^•[ ¹àæ│½Á[ • ୯ [ { } à´ & & Âà[ } ^ ^ ^ åÁ¹ Áº ã¾ } Á[ ďâ^ 원 ] @ •] @ [ ˘ • A çã • Ê çã • Ê çã • Ê çã • E • E • E • E • E • E • E • E • E • A • A • A • A • A • A • A • A • A • A • A • A • A • A • A • A • A • A • A • A • A • A • A • A • ] සංඛ්‍යා රිස රි | [ [ • #### INDICATIONS FOR USE: Ù@¬æÍ¡¡^ÑÔÚÔÁÏ^•[ ¹àæà¦^ÍÓã æð㺹ÍÓ[ ]^Ñͦæðãæ ÍøÁãßâßâßã{ Á¸Œ•] œæºÍß { [ ] [ •㺠д ] ^ Á * æð ætt ætt í í í • 7 þ. í í • 1 þ. í . • 1 ° • 1 ° • 1 ° • 1 ° • 8 á í í æ á í í æði • • 1 ° • 8 8 ° å ^ • 8 8 ° å ^ í ˜ΆΜΙã â[ } œÀи ÐæÐ½ ½ Áâ^ Ð & ©  Á - ˜Ä½¥¹½½¨¹‹Í‹¡ Œ¤ã ½­ Á¸Ç¡ · [ ç { ˆÊ´···· [ { { ˆÊ‰·¢·&q { ´ □Á ˝´Öødædã¡ Á Æ·· Çããˆ^Á æ çº) æ âºಡಾ¨ { ^} œ¤ } д [ ˆ ] æ q | ¹ ] ææã } и | œÁ } и çÁ | ″ÀJã ˘ • Áãc Á - "ÃÖˆ• Œâ½æçã㺷 Á - ˝Ά〕¹ æ½£ å Á〖 æ²ã‖[ æðã¼[ æð〠* { ^} çæã¡ } Á ## SUBSTANTIAL EQUIVALENCE: Comparison of Differences of Indication for Use to (Primary) Predicate: ປ່າໄລ *ເຂົ້າ (A § [ ] [ · · н · çã · Æ å æ å å · Å · Å å Ø Ø · Å · Æ · Å · Å · Å · Å · Å · Å · Å Å Å Å Å Å Å Å Å Å Å Å Å Å Å Å Å Å Å Å Å Å Å Å • ٱلْى ٱلْأَأَأَ ½ ٱلْ أَحْوَكُمَ } ^ أَ أَ ‫( ^ مُط ^ أَ ^ ^ مَكِه أَ [ ` • A äَ @ أَ [ ` • A äَ @ أَ [ ` • A äَ @ أَ [ ` • A äَ @ [ ] • A ä @ [ • • ] ´ • ] ´ • ] ´ • ] ´ • à[ } ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ •˜¬ãã¡ dá[ ] ^Á[ { æã } Á£ *{ ^} dí© fæç^ [æÀíãã* ^Íæс: ¡ { [ o@ v od ækçã } Ð√ @ ' ^ } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } ạ ki@Aza ^ (g c) â^âÁ xe Á½ ậ • Ậ • ̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣̣ ^ˇ˘ãçæ} of AU·lã * |æ·A¡ : (@@Aæ = ^/ } aã æ == } A¡ ! A· ^ EA র্ব | Parameters | Novabone—PRIMARY PREDICATE | SHEFABONE (SCPC) | |--------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | 510(k) # | K 040278 | pending | | Classification & ProCode | Class II, LYC | Class II, LYC | | Intended Use | Bone void filler | Bone void filler | | Indication for Use | PerioGlas - Bioglass Bone Graft<br>Particulate is indicated to be packed<br>into bony voids or gaps to fill and/or<br>augment oral, dental intraosseous, and<br>cranio~facial defects. These defects may<br>include: periodontal/infrabony defects; | ShefaBone SCPC Resorbable Bioactive Bone<br>Graft, is a silica-calcium phosphate composite,<br>synthetic bone graft material for use in oral,<br>dental intraosseous, and maxillofacial bone<br>defects. Typical uses include:<br>• Periodontal / infrabony defects | {5}------------------------------------------------ ### 510(k) Summary-Continued | Parameters | Novabone-PRIMARY PREDICATE | SHEFABONE (SCPC) | |----------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | | alveolar ridge augmentation<br>(sinusotomy, osteotomy, cystectomy);<br>dental extraction sites (ridge<br>maintenance, implant<br>preparation/placement); sinus lifts;<br>cystic defects; craniofacial<br>augmentation. PerioGlas may be used<br>alone in a manner comparable<br>to autogenous bone graft chips or<br>allograft bone particulate<br>(demineralized freeze dried bone), or it<br>may be mixed with either as a bone<br>graft extender. | • Ridge augmentation (sinusotomy, osteotomy,<br>cystectomy)<br>• Extraction sites (ridge<br>maintenance/augmentation, implant<br>preparation/ placement)<br>• Sinus lifts<br>• Cystic cavities<br>• Oral and maxillofacial augmentation | | Material Description | ionic Si, Ca, P and Na. | ionic Si, Ca, P and Na. | | | Resorbable | Resorbable | | Processing | thermal treatment to bond the<br>chemical components together | thermal treatment to bond the chemical<br>components together | | Porosity | Dense | Porous | | Particle Size | 90-710 micron | 90-710 micron | | Packaging Format | Sealed Plastic cup contains 0.5 CC or<br>Novabone Perioglass particles. Sterilized<br>by Gama radiation | Sealed glass vial contains 1 gm (1cc) of SCPC<br>particles. The vial is sealed in aluminum<br>sterilization pouch. Sterilized by Gama radiation | In addition, Shefabone SCPC is equivalent to aspects of the Reference Predicate K033611: October 1) E ÞæðÁÓ[] △ÁðÍÍ íÐÉнã Ñ' ÁнешÆÁшÐã ÁÍ Ð£ аш Ðð ( Áã ( Á) @ º) Œæ½ß″ ^) ¢¢œæðã Á §º·¢태경↑Á{ æ¹¹æďžíV®Á{ æ}Á§{ ¡ [ ] ^} ÁÇ | à DÍ ÁÙÓÚÓÁ¹Íæ}¨|^·ÁãÁæ¡ [ Áßí° · œঝಡಿ ^ÁºÍ áã' Á£áßã { Á ] @ •] @ • [ @ ] @ O O O O = ] [ ] ] • ] [ à ca | • ] ` ( ` · ) · · · · · å ( A [ / ] · / & × × ( / / / / × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × ] ✈ | | GBCOOOrg ar Occad | 760 개 = [ face / 제 / [ 1 ( 120 개 / [ 7 / 1 / 1 ( 1 / 1 / 1 / 1 / 1 / 1 / 1 / 1 / 1 / 1 / 1 / / / / / / / / / / / / / / / / / / / / / / / / / / / / aj } / } } } {{ = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = ි ç[ ãƒ í ½ð ½ ½ ½ ½ ½ ½ Í Í í ½ × Í ð þ Á × Í × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × × ai | ^ | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | ി വേണ്ടി (എ വി.) എ (എ (എ (എ (എ (എ ) ) { æ x { } [ } ^} okt í à Dj + A l = {a = = ( } } { { } } } { } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } } র্ব ## SUMMARY of TESTING/ BASIS of SUBSTANTIAL EQUIVALENCE: #### A ිරිය { æk c' අී සිත ද වි පිහි සිං දි ද ' ' œ Á™¹} Íß[] 㘠8¢ãƒ Íð£ãß Ííðãð ݽ͸ã®ÍÙÚÍFEJJHÐÚдÆÍJHÐÁÐ ÁÆÍ ншãшншãшãÁ q Áâº{ []•៤æ Á^ˇ¨ã¡¢} & ÁàæàÁÝÜÖÁæ} æˆã ÁÍ·ÁœÁÍ œº·Á§{ ] [ •ム} Áà^·[ ! Íæð åÅæð¹Á* æ{ æ • ¢¹ãã æã¡£íºÒ¯ í æ âÓ¡ ^¡··· ¸Öã] ^¦•· ã^ Á ··· ã ··· ã ··· ã Á ··· ã Á ··· ã Á ··· ã Í ·· ã | Ð ã | Ð V@Å ප්‍යැංකී වි විසින් සිට දි පිහිටු විට දි { ^æ ` ! ^ ^ ^ ^ ^ ^ ^ ^ ^ { x ^ ^ { x } ^ ^ x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x ² { ÁæFi Á ^ ^ Áj ¦^ е | е | | | • Cæ âÅ׿ßeAUOÚÖÁãÆæÐ˜ ãæà½ | * | æ \ ´æ¹·ãƒÂµ | Áæ¹ | △ | ðº ð´ | ^} Ժ¢@  æç^[ |æð.Áæ* ^ Íæet \ Áf [ o@Å ¢d ækta } н #### A CONCLUSION: #4 A ර්ශයක් | | } සින්හ { | | සැකුකු රිනු දි | | |
Innolitics
510(k) Summary
Decision Summary
Classification Order
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